Canonical Allele Identifier: CA434088158
Gene: HESX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.57232949T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.57198921T>G , CM000665.2:g.57198921T>G GRCh38
NC_000003.11:g.57232949T>G , CM000665.1:g.57232949T>G GRCh37
NC_000003.10:g.57207989T>G NCBI36
NG_008242.1:g.6332A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000295934.8:c.189A>C MANE Select ENSP00000295934.3:p.Pro63=
ENST00000647958.1:c.189A>C ENSP00000498190.1:p.Pro63=
ENST00000295934.7:c.189A>C ENSP00000295934.3:p.Pro63=
ENST00000473921.2:c.189A>C ENSP00000418918.1:p.Pro63=
ENST00000495160.2:c.189A>C ENSP00000419615.2:p.Pro63=
NM_003865.2:c.189A>C NP_003856.1:p.Pro63=
XM_005265526.3:c.189A>C XP_005265583.1:p.Pro63=
XM_006713379.2:c.189A>C XP_006713442.1:p.Pro63=
XM_011534204.1:c.189A>C XP_011532506.1:p.Pro63=
XM_011534205.1:c.189A>C XP_011532507.1:p.Pro63=
XM_005265526.4:c.189A>C XP_005265583.1:p.Pro63=
XM_011534204.2:c.189A>C XP_011532506.1:p.Pro63=
XM_011534205.2:c.189A>C XP_011532507.1:p.Pro63=
XM_017007421.1:c.189A>C XP_016862910.1:p.Pro63=
XM_024453809.1:c.189A>C XP_024309577.1:p.Pro63=
NM_003865.3:c.189A>C MANE Select NP_003856.1:p.Pro63=
NM_001376058.1:c.189A>C NP_001362987.1:p.Pro63=
NM_001376059.1:c.189A>C NP_001362988.1:p.Pro63=
NM_001376060.1:c.189A>C NP_001362989.1:p.Pro63=
NM_001376061.1:c.189A>C NP_001362990.1:p.Pro63=
NR_164757.1:n.851-429A>C