Canonical Allele Identifier: CA379112554

Gene: TH

Linked Data

• MyVariant Identifiers: chr11:g.2191101A>T (hg19) ; chr11:g.2169871A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2169871A>T , CM000673.2:g.2169871A>T	GRCh38
NC_000011.9:g.2191101A>T , CM000673.1:g.2191101A>T	GRCh37
NC_000011.8:g.2147677A>T	NCBI36
NG_008128.1:g.6935T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.91T>A MANE Select	ENSP00000325951.4:p.Ser31Thr
ENST00000324155.8:c.91-176T>A	ENSP00000325831.3:n.91-176T>A
ENST00000333684.9:c.91T>A	ENSP00000328814.6:p.Ser31Thr
ENST00000352909.7:c.91T>A	ENSP00000325951.3:p.Ser31Thr
ENST00000381168.7:c.103-176T>A	ENSP00000370560.3:n.103-176T>A
ENST00000381175.5:c.172T>A	ENSP00000370567.1:p.Ser58Thr
ENST00000381178.5:c.184T>A	ENSP00000370571.1:p.Ser62Thr
NM_000360.3:c.91T>A	NP_000351.2:p.Ser31Thr
NM_199292.2:c.184T>A	NP_954986.2:p.Ser62Thr
NM_199293.2:c.172T>A	NP_954987.2:p.Ser58Thr
XM_011520335.1:c.103T>A	XP_011518637.1:p.Ser35Thr
XM_011520335.2:c.103T>A	XP_011518637.1:p.Ser35Thr
NM_000360.4:c.91T>A MANE Select	NP_000351.2:p.Ser31Thr
NM_199292.3:c.184T>A	NP_954986.2:p.Ser62Thr
NM_199293.3:c.172T>A	NP_954987.2:p.Ser58Thr