Canonical Allele Identifier: CA1989972727

Gene: TYR

Linked Data

• dbSNP Id: rs1944769772

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89285211_89285213del , CM000673.2:g.89285211_89285213del	GRCh38
NC_000011.9:g.89018379_89018381del , CM000673.1:g.89018379_89018381del	GRCh37
NC_000011.8:g.88658027_88658029del	NCBI36
NG_008748.1:g.112340_112342del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1366+257_1366+259del MANE Select	ENSP00000263321.4:n.1366+257_1366+259del
ENST00000263321.5:c.1366+257_1366+259del	ENSP00000263321.4:n.1366+257_1366+259del
ENST00000528243.1:n.364+257_364+259del
NM_000372.4:c.1366+257_1366+259del	NP_000363.1:n.1366+257_1366+259del
XM_011542970.1:c.1366+257_1366+259del	XP_011541272.1:n.1366+257_1366+259del
XM_011542970.2:c.1366+257_1366+259del	XP_011541272.1:n.1366+257_1366+259del
XR_001748321.1:n.2456+828_2456+830del
XR_001748322.1:n.2457+828_2457+830del
NM_000372.5:c.1366+257_1366+259del MANE Select	NP_000363.1:n.1366+257_1366+259del