Canonical Allele Identifier: CA446933242

Gene: SPINK5

Linked Data

• MyVariant Identifiers: chr5:g.147486689A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148107126A>G , CM000667.2:g.148107126A>G	GRCh38
NC_000005.9:g.147486689A>G , CM000667.1:g.147486689A>G	GRCh37
NC_000005.8:g.147466882A>G	NCBI36
NG_009633.1:g.48155A>G , LRG_110:g.48155A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481286.6:n.1178A>G
ENST00000256084.8:c.1569A>G MANE Select	ENSP00000256084.7:p.Lys523=
ENST00000256084.7:c.1569A>G	ENSP00000256084.7:p.Lys523=
ENST00000359874.7:c.1569A>G	ENSP00000352936.3:p.Lys523=
ENST00000398454.5:c.1569A>G	ENSP00000381472.1:p.Lys523=
ENST00000507988.5:n.1733A>G
ENST00000508733.5:c.1512A>G	ENSP00000421519.1:p.Lys504=
NM_001127698.1:c.1569A>G	NP_001121170.1:p.Lys523=
NM_001127699.1:c.1569A>G	NP_001121171.1:p.Lys523=
NM_006846.3:c.1569A>G , LRG_110t1:c.1569A>G	NP_006837.2:p.Lys523=
XM_011537550.1:c.1512A>G	XP_011535852.1:p.Lys504=
XM_011537551.1:c.1485A>G	XP_011535853.1:p.Lys495=
XM_011537551.2:c.1485A>G	XP_011535853.1:p.Lys495=
NM_001127698.2:c.1569A>G	NP_001121170.1:p.Lys523=
NM_001127699.2:c.1569A>G	NP_001121171.1:p.Lys523=
NM_006846.4:c.1569A>G MANE Select	NP_006837.2:p.Lys523=