Canonical Allele Identifier: CA2793087785

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178909C>T , CM000673.2:g.89178909C>T	GRCh38
NC_000011.9:g.88912077C>T , CM000673.1:g.88912077C>T	GRCh37
NC_000011.8:g.88551725C>T	NCBI36
NG_008748.1:g.6038C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+137C>T MANE Select	ENSP00000263321.4:n.819+137C>T
ENST00000263321.5:c.819+137C>T	ENSP00000263321.4:n.819+137C>T
ENST00000526139.1:n.880+137C>T
NM_000372.4:c.819+137C>T	NP_000363.1:n.819+137C>T
XM_011542970.1:c.819+137C>T	XP_011541272.1:n.819+137C>T
XM_011542970.2:c.819+137C>T	XP_011541272.1:n.819+137C>T
XR_001748321.1:n.2718-65376G>A
XR_001748322.1:n.2733-65376G>A
NM_000372.5:c.819+137C>T MANE Select	NP_000363.1:n.819+137C>T