Canonical Allele Identifier: CA377538801

Gene: HTR7

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.90857261G>C , CM000672.2:g.90857261G>C	GRCh38
NC_000010.10:g.92617018G>C , CM000672.1:g.92617018G>C	GRCh37
NC_000010.9:g.92606998G>C	NCBI36
NG_029218.1:g.5654C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_019859.4:c.411C>G MANE Select	NP_062873.1:p.Phe137Leu
ENST00000336152.8:c.411C>G MANE Select	ENSP00000337949.3:p.Phe137Leu
NM_000872.4:c.411C>G	NP_000863.1:p.Phe137Leu
NM_000872.5:c.411C>G	NP_000863.1:p.Phe137Leu
NM_019859.3:c.411C>G	NP_062873.1:p.Phe137Leu
NM_019860.3:c.411C>G	NP_062874.1:p.Phe137Leu
NM_019860.4:c.411C>G	NP_062874.1:p.Phe137Leu
ENST00000277874.10:c.411C>G	ENSP00000277874.6:p.Phe137Leu
ENST00000336152.7:c.411C>G	ENSP00000337949.3:p.Phe137Leu
ENST00000371719.2:c.411C>G	ENSP00000360784.2:p.Phe137Leu