Canonical Allele Identifier: CA379126700

Gene: TH

Linked Data

• gnomAD v4: 11-2166935-G-A
• MyVariant Identifiers: chr11:g.2188165G>A (hg19) ; chr11:g.2166935G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2166935G>A , CM000673.2:g.2166935G>A	GRCh38
NC_000011.9:g.2188165G>A , CM000673.1:g.2188165G>A	GRCh37
NC_000011.8:g.2144741G>A	NCBI36
NG_008128.1:g.9871C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.793C>T MANE Select	ENSP00000325951.4:p.Arg265Trp
ENST00000324155.8:c.*482C>T	ENSP00000325831.3:n.*482C>T
ENST00000333684.9:c.696-386C>T	ENSP00000328814.6:n.696-386C>T
ENST00000352909.7:c.793C>T	ENSP00000325951.3:p.Arg265Trp
ENST00000381168.7:c.*513C>T	ENSP00000370560.3:n.*513C>T
ENST00000381175.5:c.874C>T	ENSP00000370567.1:p.Arg292Trp
ENST00000381178.5:c.886C>T	ENSP00000370571.1:p.Arg296Trp
ENST00000412076.1:c.136-386C>T
ENST00000416223.5:c.136-167C>T
ENST00000469226.1:n.922C>T
ENST00000479437.5:n.342C>T
NM_000360.3:c.793C>T	NP_000351.2:p.Arg265Trp
NM_199292.2:c.886C>T	NP_954986.2:p.Arg296Trp
NM_199293.2:c.874C>T	NP_954987.2:p.Arg292Trp
XM_011520335.1:c.805C>T	XP_011518637.1:p.Arg269Trp
XM_011520335.2:c.805C>T	XP_011518637.1:p.Arg269Trp
NM_000360.4:c.793C>T MANE Select	NP_000351.2:p.Arg265Trp
NM_199292.3:c.886C>T	NP_954986.2:p.Arg296Trp
NM_199293.3:c.874C>T	NP_954987.2:p.Arg292Trp