Canonical Allele Identifier: CA3496214

Gene: SPINK5

Linked Data

• dbSNP Id: rs192473445
• ExAC: 5:147510846 C / A
• gnomAD v2: 5-147510846-C-A
• gnomAD v3: 5-148131283-C-A
• gnomAD v4: 5-148131283-C-A
• MyVariant Identifiers: chr5:g.147510846C>A (hg19) ; chr5:g.148131283C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148131283C>A , CM000667.2:g.148131283C>A	GRCh38
NC_000005.9:g.147510846C>A , CM000667.1:g.147510846C>A	GRCh37
NC_000005.8:g.147491039C>A	NCBI36
NG_009633.1:g.72312C>A , LRG_110:g.72312C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256084.8:c.2989C>A MANE Select	ENSP00000256084.7:p.Arg997=
ENST00000256084.7:c.2989C>A	ENSP00000256084.7:p.Arg997=
ENST00000359874.7:c.3079C>A	ENSP00000352936.3:p.Arg1027=
NM_001127698.1:c.3079C>A	NP_001121170.1:p.Arg1027=
NM_006846.3:c.2989C>A , LRG_110t1:c.2989C>A	NP_006837.2:p.Arg997=
XM_011537550.1:c.3022C>A	XP_011535852.1:p.Arg1008=
XM_011537551.1:c.2995C>A	XP_011535853.1:p.Arg999=
XM_011537551.2:c.2995C>A	XP_011535853.1:p.Arg999=
NM_001127698.2:c.3079C>A	NP_001121170.1:p.Arg1027=
NM_006846.4:c.2989C>A MANE Select	NP_006837.2:p.Arg997=