Canonical Allele Identifier: CA1589887389

Gene: SPINK5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148095907T= , CM000667.2:g.148095907T=	GRCh38
NC_000005.9:g.147475470T= , CM000667.1:g.147475470T=	GRCh37
NC_000005.8:g.147455663T=	NCBI36
NG_009633.1:g.36936T= , LRG_110:g.36936T=

Transcript Alleles

HGVS	Amino-acid Change
NM_006846.4:c.882+2T= MANE Select	NP_006837.2:n.882+2T=
ENST00000256084.8:c.882+2T= MANE Select	ENSP00000256084.7:n.882+2T=
NM_001127698.1:c.882+2T=	NP_001121170.1:n.882+2T=
NM_001127698.2:c.882+2T=	NP_001121170.1:n.882+2T=
NM_001127699.1:c.882+2T=	NP_001121171.1:n.882+2T=
NM_001127699.2:c.882+2T=	NP_001121171.1:n.882+2T=
NM_006846.3:c.882+2T= , LRG_110t1:c.882+2T=	NP_006837.2:n.882+2T=
ENST00000256084.7:c.882+2T=	ENSP00000256084.7:n.882+2T=
ENST00000359874.7:c.882+2T=	ENSP00000352936.3:n.882+2T=
ENST00000398454.5:c.882+2T=	ENSP00000381472.1:n.882+2T=
ENST00000476608.1:n.398+2T=
ENST00000481286.5:n.328+2T=
ENST00000481286.6:n.491+2T=
ENST00000507988.5:n.1046+2T=
ENST00000508733.5:c.825+2T=	ENSP00000421519.1:n.825+2T=
ENST00000698105.1:n.752+2T=
XM_011537550.1:c.825+2T=	XP_011535852.1:n.825+2T=
XM_011537551.1:c.798+2T=	XP_011535853.1:n.798+2T=
XM_011537551.2:c.798+2T=	XP_011535853.1:n.798+2T=