Canonical Allele Identifier: CA4261585

Gene: FIGNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.50445390G>A , CM000669.2:g.50445390G>A	GRCh38
NC_000007.13:g.50513088G>A , CM000669.1:g.50513088G>A	GRCh37
NC_000007.12:g.50480582G>A	NCBI36
NG_051949.1:g.10017C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001287492.4:c.1898C>T MANE Select	NP_001274421.1:p.Pro633Leu
ENST00000433017.6:c.1898C>T MANE Select	ENSP00000399997.1:p.Pro633Leu
NM_001042762.2:c.1898C>T	NP_001036227.1:p.Pro633Leu
NM_001042762.3:c.1898C>T	NP_001036227.1:p.Pro633Leu
NM_001042762.4:c.1898C>T	NP_001036227.1:p.Pro633Leu
NM_001042762.5:c.1898C>T	NP_001036227.1:p.Pro633Leu
NM_001287492.1:c.1898C>T	NP_001274421.1:p.Pro633Leu
NM_001287492.2:c.1898C>T	NP_001274421.1:p.Pro633Leu
NM_001287492.3:c.1898C>T	NP_001274421.1:p.Pro633Leu
NM_001287493.1:c.1898C>T	NP_001274422.1:p.Pro633Leu
NM_001287493.2:c.1898C>T	NP_001274422.1:p.Pro633Leu
NM_001287493.3:c.1898C>T	NP_001274422.1:p.Pro633Leu
NM_001287494.1:c.1898C>T	NP_001274423.1:p.Pro633Leu
NM_001287494.2:c.1898C>T	NP_001274423.1:p.Pro633Leu
NM_001287494.3:c.1898C>T	NP_001274423.1:p.Pro633Leu
NM_001287494.4:c.1898C>T	NP_001274423.1:p.Pro633Leu
NM_001287495.1:c.1898C>T	NP_001274424.1:p.Pro633Leu
NM_001287495.2:c.1898C>T	NP_001274424.1:p.Pro633Leu
NM_001287495.3:c.1898C>T	NP_001274424.1:p.Pro633Leu
NM_001287496.1:c.1565C>T	NP_001274425.1:p.Pro522Leu
NM_001287496.2:c.1565C>T	NP_001274425.1:p.Pro522Leu
NM_001287496.3:c.1565C>T	NP_001274425.1:p.Pro522Leu
NM_001287496.4:c.1565C>T	NP_001274425.1:p.Pro522Leu
NM_001346558.1:c.1565C>T	NP_001333487.1:p.Pro522Leu
NM_001346558.2:c.1565C>T	NP_001333487.1:p.Pro522Leu
NM_001346558.3:c.1565C>T	NP_001333487.1:p.Pro522Leu
NM_001346559.1:c.1565C>T	NP_001333488.1:p.Pro522Leu
NM_001346559.2:c.1565C>T	NP_001333488.1:p.Pro522Leu
NM_001346559.3:c.1565C>T	NP_001333488.1:p.Pro522Leu
NM_001346560.1:c.1898C>T	NP_001333489.1:p.Pro633Leu
NM_001346560.2:c.1898C>T	NP_001333489.1:p.Pro633Leu
NM_001346560.3:c.1898C>T	NP_001333489.1:p.Pro633Leu
NM_001346561.1:c.1898C>T	NP_001333490.1:p.Pro633Leu
NM_001346561.2:c.1898C>T	NP_001333490.1:p.Pro633Leu
NM_001346561.3:c.1898C>T	NP_001333490.1:p.Pro633Leu
NM_001346562.1:c.1898C>T	NP_001333491.1:p.Pro633Leu
NM_001346562.2:c.1898C>T	NP_001333491.1:p.Pro633Leu
NM_001346562.3:c.1898C>T	NP_001333491.1:p.Pro633Leu
NM_001346563.1:c.1898C>T	NP_001333492.1:p.Pro633Leu
NM_001346563.2:c.1898C>T	NP_001333492.1:p.Pro633Leu
NM_001346563.3:c.1898C>T	NP_001333492.1:p.Pro633Leu
NM_001346564.1:c.1898C>T	NP_001333493.1:p.Pro633Leu
NM_001346564.2:c.1898C>T	NP_001333493.1:p.Pro633Leu
NM_001346564.3:c.1898C>T	NP_001333493.1:p.Pro633Leu
NM_001346565.1:c.1898C>T	NP_001333494.1:p.Pro633Leu
NM_001346565.2:c.1898C>T	NP_001333494.1:p.Pro633Leu
NM_001346565.3:c.1898C>T	NP_001333494.1:p.Pro633Leu
NM_022116.4:c.1898C>T	NP_071399.2:p.Pro633Leu
NM_022116.5:c.1898C>T	NP_071399.2:p.Pro633Leu
NM_022116.6:c.1898C>T	NP_071399.2:p.Pro633Leu
NM_022116.7:c.1898C>T	NP_071399.2:p.Pro633Leu
ENST00000356889.8:c.1898C>T	ENSP00000349356.4:p.Pro633Leu
ENST00000395556.6:c.1898C>T	ENSP00000378924.2:p.Pro633Leu
ENST00000419119.1:c.1898C>T	ENSP00000410811.1:p.Pro633Leu
ENST00000433017.5:c.1898C>T	ENSP00000399997.1:p.Pro633Leu
ENST00000611938.4:c.1898C>T	ENSP00000484551.1:p.Pro633Leu
ENST00000613602.3:c.1898C>T	ENSP00000481751.1:p.Pro633Leu
ENST00000615084.4:c.1898C>T	ENSP00000483543.1:p.Pro633Leu
ENST00000617389.4:c.1898C>T	ENSP00000483126.1:p.Pro633Leu
XM_005271783.1:c.1565C>T	XP_005271840.1:p.Pro522Leu
XM_011515469.1:c.1898C>T	XP_011513771.1:p.Pro633Leu
XM_011515470.1:c.1898C>T	XP_011513772.1:p.Pro633Leu
XM_011515470.3:c.1898C>T	XP_011513772.1:p.Pro633Leu
XM_011515471.1:c.1898C>T	XP_011513773.1:p.Pro633Leu
XM_011515472.1:c.1565C>T	XP_011513774.1:p.Pro522Leu
XM_017012501.1:c.1898C>T	XP_016867990.1:p.Pro633Leu
XM_024446863.1:c.1898C>T	XP_024302631.1:p.Pro633Leu
XM_024446864.1:c.1898C>T	XP_024302632.1:p.Pro633Leu
XM_024446865.1:c.1898C>T	XP_024302633.1:p.Pro633Leu