Canonical Allele Identifier: CA361651938

Gene: SPINK5

Linked Data

• COSMIC: COSM1063996 ; COSM1063997
• MyVariant Identifiers: chr5:g.147510838A>G (hg19) ; chr5:g.148131275A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148131275A>G , CM000667.2:g.148131275A>G	GRCh38
NC_000005.9:g.147510838A>G , CM000667.1:g.147510838A>G	GRCh37
NC_000005.8:g.147491031A>G	NCBI36
NG_009633.1:g.72304A>G , LRG_110:g.72304A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256084.8:c.2981A>G MANE Select	ENSP00000256084.7:p.Lys994Arg
ENST00000256084.7:c.2981A>G	ENSP00000256084.7:p.Lys994Arg
ENST00000359874.7:c.3071A>G	ENSP00000352936.3:p.Lys1024Arg
NM_001127698.1:c.3071A>G	NP_001121170.1:p.Lys1024Arg
NM_006846.3:c.2981A>G , LRG_110t1:c.2981A>G	NP_006837.2:p.Lys994Arg
XM_011537550.1:c.3014A>G	XP_011535852.1:p.Lys1005Arg
XM_011537551.1:c.2987A>G	XP_011535853.1:p.Lys996Arg
XM_011537551.2:c.2987A>G	XP_011535853.1:p.Lys996Arg
NM_001127698.2:c.3071A>G	NP_001121170.1:p.Lys1024Arg
NM_006846.4:c.2981A>G MANE Select	NP_006837.2:p.Lys994Arg