Canonical Allele Identifier: CA1589892195

Gene: SPINK5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148107114C= , CM000667.2:g.148107114C=	GRCh38
NC_000005.9:g.147486677C= , CM000667.1:g.147486677C=	GRCh37
NC_000005.8:g.147466870C=	NCBI36
NG_009633.1:g.48143C= , LRG_110:g.48143C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481286.6:n.1166C=
ENST00000256084.8:c.1557C= MANE Select	ENSP00000256084.7:p.Gly519=
ENST00000256084.7:c.1557C=	ENSP00000256084.7:p.Gly519=
ENST00000359874.7:c.1557C=	ENSP00000352936.3:p.Gly519=
ENST00000398454.5:c.1557C=	ENSP00000381472.1:p.Gly519=
ENST00000507988.5:n.1721C=
ENST00000508733.5:c.1500C=	ENSP00000421519.1:p.Gly500=
NM_001127698.1:c.1557C=	NP_001121170.1:p.Gly519=
NM_001127699.1:c.1557C=	NP_001121171.1:p.Gly519=
NM_006846.3:c.1557C= , LRG_110t1:c.1557C=	NP_006837.2:p.Gly519=
XM_011537550.1:c.1500C=	XP_011535852.1:p.Gly500=
XM_011537551.1:c.1473C=	XP_011535853.1:p.Gly491=
XM_011537551.2:c.1473C=	XP_011535853.1:p.Gly491=
NM_001127698.2:c.1557C=	NP_001121170.1:p.Gly519=
NM_001127699.2:c.1557C=	NP_001121171.1:p.Gly519=
NM_006846.4:c.1557C= MANE Select	NP_006837.2:p.Gly519=