Canonical Allele Identifier: CA1927461586

Gene: HTR7

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.90834586C= , CM000672.2:g.90834586C=	GRCh38
NC_000010.10:g.92594343C= , CM000672.1:g.92594343C=	GRCh37
NC_000010.9:g.92584323C=	NCBI36
NG_029218.1:g.28329G=

Transcript Alleles

HGVS	Amino-acid Change
NM_019859.4:c.539+22547G= MANE Select	NP_062873.1:n.539+22547G=
ENST00000336152.8:c.539+22547G= MANE Select	ENSP00000337949.3:n.539+22547G=
NM_000872.4:c.539+22547G=	NP_000863.1:n.539+22547G=
NM_000872.5:c.539+22547G=	NP_000863.1:n.539+22547G=
NM_019859.3:c.539+22547G=	NP_062873.1:n.539+22547G=
NM_019860.3:c.539+22547G=	NP_062874.1:n.539+22547G=
NM_019860.4:c.539+22547G=	NP_062874.1:n.539+22547G=
ENST00000277874.10:c.539+22547G=	ENSP00000277874.6:n.539+22547G=
ENST00000336152.7:c.539+22547G=	ENSP00000337949.3:n.539+22547G=
ENST00000371719.2:c.539+22547G=	ENSP00000360784.2:n.539+22547G=