Canonical Allele Identifier: CA377538811

Gene: HTR7

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.90857263A>G , CM000672.2:g.90857263A>G	GRCh38
NC_000010.10:g.92617020A>G , CM000672.1:g.92617020A>G	GRCh37
NC_000010.9:g.92607000A>G	NCBI36
NG_029218.1:g.5652T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_019859.4:c.409T>C MANE Select	NP_062873.1:p.Phe137Leu
ENST00000336152.8:c.409T>C MANE Select	ENSP00000337949.3:p.Phe137Leu
NM_000872.4:c.409T>C	NP_000863.1:p.Phe137Leu
NM_000872.5:c.409T>C	NP_000863.1:p.Phe137Leu
NM_019859.3:c.409T>C	NP_062873.1:p.Phe137Leu
NM_019860.3:c.409T>C	NP_062874.1:p.Phe137Leu
NM_019860.4:c.409T>C	NP_062874.1:p.Phe137Leu
ENST00000277874.10:c.409T>C	ENSP00000277874.6:p.Phe137Leu
ENST00000336152.7:c.409T>C	ENSP00000337949.3:p.Phe137Leu
ENST00000371719.2:c.409T>C	ENSP00000360784.2:p.Phe137Leu