Canonical Allele Identifier: CA75378646

Gene: HESX1

Linked Data

• dbSNP Id: rs938365060
• gnomAD v2: 3-57232181-A-G
• gnomAD v3: 3-57198153-A-G
• gnomAD v4: 3-57198153-A-G
• MyVariant Identifiers: chr3:g.57232181A>G (hg19) ; chr3:g.57198153A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.57198153A>G , CM000665.2:g.57198153A>G	GRCh38
NC_000003.11:g.57232181A>G , CM000665.1:g.57232181A>G	GRCh37
NC_000003.10:g.57207221A>G	NCBI36
NG_008242.1:g.7100T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295934.8:c.*44T>C MANE Select	ENSP00000295934.3:n.*44T>C
ENST00000647958.1:c.*44T>C	ENSP00000498190.1:n.*44T>C
ENST00000295934.7:c.*44T>C	ENSP00000295934.3:n.*44T>C
ENST00000473921.2:c.*44T>C	ENSP00000418918.1:n.*44T>C
NM_003865.2:c.*44T>C	NP_003856.1:n.*44T>C
XM_005265526.3:c.*44T>C	XP_005265583.1:n.*44T>C
XM_006713379.2:c.*44T>C	XP_006713442.1:n.*44T>C
XM_011534204.1:c.*44T>C	XP_011532506.1:n.*44T>C
XM_011534205.1:c.*44T>C	XP_011532507.1:n.*44T>C
XM_005265526.4:c.*44T>C	XP_005265583.1:n.*44T>C
XM_011534204.2:c.*44T>C	XP_011532506.1:n.*44T>C
XM_011534205.2:c.*44T>C	XP_011532507.1:n.*44T>C
XM_017007421.1:c.*44T>C	XP_016862910.1:n.*44T>C
XM_024453809.1:c.*44T>C	XP_024309577.1:n.*44T>C
NM_003865.3:c.*44T>C MANE Select	NP_003856.1:n.*44T>C
NM_001376058.1:c.*44T>C	NP_001362987.1:n.*44T>C
NM_001376059.1:c.*44T>C	NP_001362988.1:n.*44T>C
NM_001376060.1:c.*44T>C	NP_001362989.1:n.*44T>C
NM_001376061.1:c.*44T>C	NP_001362990.1:n.*44T>C
NR_164757.1:n.1095T>C