Canonical Allele Identifier: CA361652267

Gene: SPINK5

Linked Data

• ClinVar Variation Id: 655194
• ClinVar RCV Id: RCV003596600
• dbSNP Id: rs1581113847
• MyVariant Identifiers: chr5:g.147510948A>G (hg19) ; chr5:g.148131385A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148131385A>G , CM000667.2:g.148131385A>G	GRCh38
NC_000005.9:g.147510948A>G , CM000667.1:g.147510948A>G	GRCh37
NC_000005.8:g.147491141A>G	NCBI36
NG_009633.1:g.72414A>G , LRG_110:g.72414A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256084.8:c.3091A>G MANE Select	ENSP00000256084.7:p.Asn1031Asp
ENST00000256084.7:c.3091A>G	ENSP00000256084.7:p.Asn1031Asp
ENST00000359874.7:c.3181A>G	ENSP00000352936.3:p.Asn1061Asp
NM_001127698.1:c.3181A>G	NP_001121170.1:p.Asn1061Asp
NM_006846.3:c.3091A>G , LRG_110t1:c.3091A>G	NP_006837.2:p.Asn1031Asp
XM_011537550.1:c.3124A>G	XP_011535852.1:p.Asn1042Asp
XM_011537551.1:c.3097A>G	XP_011535853.1:p.Asn1033Asp
XM_011537551.2:c.3097A>G	XP_011535853.1:p.Asn1033Asp
NM_001127698.2:c.3181A>G	NP_001121170.1:p.Asn1061Asp
NM_006846.4:c.3091A>G MANE Select	NP_006837.2:p.Asn1031Asp