Canonical Allele Identifier: CA361652118

Gene: SPINK5

Linked Data

• MyVariant Identifiers: chr5:g.147510884T>G (hg19) ; chr5:g.148131321T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148131321T>G , CM000667.2:g.148131321T>G	GRCh38
NC_000005.9:g.147510884T>G , CM000667.1:g.147510884T>G	GRCh37
NC_000005.8:g.147491077T>G	NCBI36
NG_009633.1:g.72350T>G , LRG_110:g.72350T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256084.8:c.3027T>G MANE Select	ENSP00000256084.7:p.Asp1009Glu
ENST00000256084.7:c.3027T>G	ENSP00000256084.7:p.Asp1009Glu
ENST00000359874.7:c.3117T>G	ENSP00000352936.3:p.Asp1039Glu
NM_001127698.1:c.3117T>G	NP_001121170.1:p.Asp1039Glu
NM_006846.3:c.3027T>G , LRG_110t1:c.3027T>G	NP_006837.2:p.Asp1009Glu
XM_011537550.1:c.3060T>G	XP_011535852.1:p.Asp1020Glu
XM_011537551.1:c.3033T>G	XP_011535853.1:p.Asp1011Glu
XM_011537551.2:c.3033T>G	XP_011535853.1:p.Asp1011Glu
NM_001127698.2:c.3117T>G	NP_001121170.1:p.Asp1039Glu
NM_006846.4:c.3027T>G MANE Select	NP_006837.2:p.Asp1009Glu