Canonical Allele Identifier: CA2615484146

Gene: TYR

Linked Data

• gnomAD v4: 11-89284709-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89284709A>C , CM000673.2:g.89284709A>C	GRCh38
NC_000011.9:g.89017877A>C , CM000673.1:g.89017877A>C	GRCh37
NC_000011.8:g.88657525A>C	NCBI36
NG_008748.1:g.111838A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000263321.6:c.1185-64A>C MANE Select	ENSP00000263321.4:n.1185-64A>C
ENST00000263321.5:c.1185-64A>C	ENSP00000263321.4:n.1185-64A>C
ENST00000528243.1:n.183-64A>C
NM_000372.4:c.1185-64A>C	NP_000363.1:n.1185-64A>C
XM_011542970.1:c.1185-64A>C	XP_011541272.1:n.1185-64A>C
XM_011542970.2:c.1185-64A>C	XP_011541272.1:n.1185-64A>C
XR_001748321.1:n.2456+1325T>G
XR_001748322.1:n.2457+1325T>G
NM_000372.5:c.1185-64A>C MANE Select	NP_000363.1:n.1185-64A>C