Canonical Allele Identifier: CA1201568183

Gene: SPTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158685311_158685312delinsCT , CM000663.2:g.158685311_158685312delinsCT	GRCh38
NC_000001.10:g.158655101_158655102delinsCT , CM000663.1:g.158655101_158655102delinsCT	GRCh37
NC_000001.9:g.156921725_156921726delinsCT	NCBI36
NG_011474.1:g.6405_6406delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643759.2:c.60_61delinsAG MANE Select	ENSP00000495214.1:p.Thr20=
ENST00000368147.8:c.60_61delinsAG	ENSP00000357129.4:p.Thr20=
ENST00000467387.1:c.60_61delinsAG	ENSP00000476485.1:p.Thr20=
ENST00000614909.4:c.60_61delinsAG	ENSP00000482595.1:p.Thr20=
NM_003126.2:c.60_61delinsAG	NP_003117.2:p.Thr20=
XM_011509916.1:c.60_61delinsAG	XP_011508218.1:p.Thr20=
XM_011509917.1:c.60_61delinsAG	XP_011508219.1:p.Thr20=
XM_011509918.1:c.60_61delinsAG	XP_011508220.1:p.Thr20=
XM_011509919.1:c.60_61delinsAG	XP_011508221.1:p.Thr20=
XR_921911.1:n.173_174delinsAG
XR_921912.1:n.178_179delinsAG
NM_003126.3:c.60_61delinsAG	NP_003117.2:p.Thr20=
XM_011509916.2:c.60_61delinsAG	XP_011508218.1:p.Thr20=
XM_011509917.3:c.60_61delinsAG	XP_011508219.1:p.Thr20=
XM_011509918.3:c.60_61delinsAG	XP_011508220.1:p.Thr20=
XM_011509919.3:c.60_61delinsAG	XP_011508221.1:p.Thr20=
XR_921911.3:n.186_187delinsAG
XR_921912.2:n.188_189delinsAG
NM_003126.4:c.60_61delinsAG MANE Select	NP_003117.2:p.Thr20=