Canonical Allele Identifier: CA379112742

Gene: TH

Linked Data

• MyVariant Identifiers: chr11:g.2192921T>G (hg19) ; chr11:g.2171691T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2171691T>G , CM000673.2:g.2171691T>G	GRCh38
NC_000011.9:g.2192921T>G , CM000673.1:g.2192921T>G	GRCh37
NC_000011.8:g.2149497T>G	NCBI36
NG_008128.1:g.5115A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000352909.8:c.90+6A>C MANE Select	ENSP00000325951.4:n.90+6A>C
ENST00000324155.8:c.90+6A>C	ENSP00000325831.3:n.90+6A>C
ENST00000333684.9:c.90+6A>C	ENSP00000328814.6:n.90+6A>C
ENST00000352909.7:c.90+6A>C	ENSP00000325951.3:n.90+6A>C
ENST00000381168.7:c.96A>C	ENSP00000370560.3:p.Arg32Ser
ENST00000381175.5:c.90+6A>C	ENSP00000370567.1:n.90+6A>C
ENST00000381178.5:c.96A>C	ENSP00000370571.1:p.Arg32Ser
NM_000360.3:c.90+6A>C	NP_000351.2:n.90+6A>C
NM_199292.2:c.96A>C	NP_954986.2:p.Arg32Ser
NM_199293.2:c.90+6A>C	NP_954987.2:n.90+6A>C
XM_011520335.1:c.96A>C	XP_011518637.1:p.Arg32Ser
XM_011520335.2:c.96A>C	XP_011518637.1:p.Arg32Ser
NM_000360.4:c.90+6A>C MANE Select	NP_000351.2:n.90+6A>C
NM_199292.3:c.96A>C	NP_954986.2:p.Arg32Ser
NM_199293.3:c.90+6A>C	NP_954987.2:n.90+6A>C