Canonical Allele Identifier: CA3096687170

Gene: SPATS2L

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.200449512A= , CM000664.2:g.200449512A=	GRCh38
NC_000002.11:g.201314235A= , CM000664.1:g.201314235A=	GRCh37
NC_000002.10:g.201022480A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001100423.2:c.788+8728A= MANE Select	NP_001093893.1:n.788+8728A=
ENST00000409140.8:c.788+8728A= MANE Select	ENSP00000386730.3:n.788+8728A=
NM_001100422.1:c.788+8728A=	NP_001093892.1:n.788+8728A=
NM_001100423.1:c.788+8728A=	NP_001093893.1:n.788+8728A=
NM_001100424.1:c.581+8728A=	NP_001093894.1:n.581+8728A=
NM_001282735.1:c.788+8728A=	NP_001269664.1:n.788+8728A=
NM_001282743.1:c.608+8728A=	NP_001269672.1:n.608+8728A=
NM_001282744.1:c.878+8728A=	NP_001269673.1:n.878+8728A=
NM_001282744.2:c.878+8728A=	NP_001269673.1:n.878+8728A=
NM_015535.2:c.788+8728A=	NP_056350.2:n.788+8728A=
NM_015535.3:c.788+8728A=	NP_056350.2:n.788+8728A=
ENST00000358677.9:c.788+8728A=	ENSP00000351503.4:n.788+8728A=
ENST00000360760.9:c.581+8728A=	ENSP00000353989.5:n.581+8728A=
ENST00000366118.2:c.136+8728A=
ENST00000409140.7:c.788+8728A=	ENSP00000386730.3:n.788+8728A=
ENST00000409151.5:c.812+8728A=	ENSP00000386310.1:n.812+8728A=
ENST00000409385.5:c.608+8728A=	ENSP00000386391.1:n.608+8728A=
ENST00000409397.6:c.581+8728A=	ENSP00000386600.2:n.581+8728A=
ENST00000409718.5:c.788+8728A=	ENSP00000386336.1:n.788+8728A=
ENST00000409755.7:c.539+8728A=	ENSP00000387333.4:n.539+8728A=
ENST00000409988.7:c.788+8728A=	ENSP00000386931.3:n.788+8728A=
ENST00000438761.5:c.566+8728A=	ENSP00000413648.1:n.566+8728A=
ENST00000451764.6:c.788+8728A=	ENSP00000391467.2:n.788+8728A=
ENST00000619961.4:c.878+8728A=	ENSP00000482515.1:n.878+8728A=
XM_005246456.1:c.788+8728A=	XP_005246513.1:n.788+8728A=
XM_005246457.1:c.788+8728A=	XP_005246514.1:n.788+8728A=
XM_005246458.1:c.788+8728A=	XP_005246515.1:n.788+8728A=
XM_005246458.2:c.788+8728A=	XP_005246515.1:n.788+8728A=
XM_005246459.1:c.581+8728A=	XP_005246516.1:n.581+8728A=
XM_011510938.1:c.878+8728A=	XP_011509240.1:n.878+8728A=
XM_011510939.1:c.788+8728A=	XP_011509241.1:n.788+8728A=
XM_011510940.1:c.581+8728A=	XP_011509242.1:n.581+8728A=
XM_017003784.2:c.671+8728A=	XP_016859273.1:n.671+8728A=
XM_017003785.2:c.581+8728A=	XP_016859274.1:n.581+8728A=
XM_017003786.1:c.581+8728A=	XP_016859275.1:n.581+8728A=
XM_017003787.1:c.581+8728A=	XP_016859276.1:n.581+8728A=
XM_024452785.1:c.788+8728A=	XP_024308553.1:n.788+8728A=
XM_024452786.1:c.788+8728A=	XP_024308554.1:n.788+8728A=
XM_024452787.1:c.788+8728A=	XP_024308555.1:n.788+8728A=
XM_024452788.1:c.581+8728A=	XP_024308556.1:n.581+8728A=
XR_001739165.2:n.642-44T=
XR_001739166.2:n.428-17975T=
XR_001739167.1:n.642-17975T=
XR_241386.3:n.1535-44T=
XR_241387.3:n.231-44T=
XR_923779.1:n.1535-44T=
XR_923780.1:n.1535-44T=
XR_923781.1:n.1535-17975T=
XR_923782.1:n.1535-19875T=