Canonical Allele Identifier: CA1589876992

Gene: SPINK5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148070377C= , CM000667.2:g.148070377C=	GRCh38
NC_000005.9:g.147449940C= , CM000667.1:g.147449940C=	GRCh37
NC_000005.8:g.147430133C=	NCBI36
NG_009633.1:g.11406C= , LRG_110:g.11406C=

Transcript Alleles

HGVS	Amino-acid Change
NM_006846.4:c.136C= MANE Select	NP_006837.2:p.Gln46=
ENST00000256084.8:c.136C= MANE Select	ENSP00000256084.7:p.Gln46=
NM_001127698.1:c.136C=	NP_001121170.1:p.Gln46=
NM_001127698.2:c.136C=	NP_001121170.1:p.Gln46=
NM_001127699.1:c.136C=	NP_001121171.1:p.Gln46=
NM_001127699.2:c.136C=	NP_001121171.1:p.Gln46=
NM_006846.3:c.136C= , LRG_110t1:c.136C=	NP_006837.2:p.Gln46=
ENST00000256084.7:c.136C=	ENSP00000256084.7:p.Gln46=
ENST00000359874.7:c.136C=	ENSP00000352936.3:p.Gln46=
ENST00000398454.5:c.136C=	ENSP00000381472.1:p.Gln46=
ENST00000476697.7:c.136C=	ENSP00000427943.1:p.Gln46=
ENST00000507988.5:n.300C=
ENST00000508733.5:c.82-3C=	ENSP00000421519.1:n.82-3C=
ENST00000521206.5:c.82-3C=	ENSP00000430264.1:n.82-3C=
XM_011537550.1:c.82-3C=	XP_011535852.1:n.82-3C=
XM_011537551.1:c.52C=	XP_011535853.1:p.Gln18=
XM_011537551.2:c.52C=	XP_011535853.1:p.Gln18=