Canonical Allele Identifier: CA353401550

Gene: HESX1

Linked Data

• MyVariant Identifiers: chr3:g.57232947T>A (hg19) ; chr3:g.57198919T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.57198919T>A , CM000665.2:g.57198919T>A	GRCh38
NC_000003.11:g.57232947T>A , CM000665.1:g.57232947T>A	GRCh37
NC_000003.10:g.57207987T>A	NCBI36
NG_008242.1:g.6334A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295934.8:c.191A>T MANE Select	ENSP00000295934.3:p.Asn64Ile
ENST00000647958.1:c.191A>T	ENSP00000498190.1:p.Asn64Ile
ENST00000295934.7:c.191A>T	ENSP00000295934.3:p.Asn64Ile
ENST00000473921.2:c.191A>T	ENSP00000418918.1:p.Asn64Ile
ENST00000495160.2:c.191A>T	ENSP00000419615.2:p.Asn64Ile
NM_003865.2:c.191A>T	NP_003856.1:p.Asn64Ile
XM_005265526.3:c.191A>T	XP_005265583.1:p.Asn64Ile
XM_006713379.2:c.191A>T	XP_006713442.1:p.Asn64Ile
XM_011534204.1:c.191A>T	XP_011532506.1:p.Asn64Ile
XM_011534205.1:c.191A>T	XP_011532507.1:p.Asn64Ile
XM_005265526.4:c.191A>T	XP_005265583.1:p.Asn64Ile
XM_011534204.2:c.191A>T	XP_011532506.1:p.Asn64Ile
XM_011534205.2:c.191A>T	XP_011532507.1:p.Asn64Ile
XM_017007421.1:c.191A>T	XP_016862910.1:p.Asn64Ile
XM_024453809.1:c.191A>T	XP_024309577.1:p.Asn64Ile
NM_003865.3:c.191A>T MANE Select	NP_003856.1:p.Asn64Ile
NM_001376058.1:c.191A>T	NP_001362987.1:p.Asn64Ile
NM_001376059.1:c.191A>T	NP_001362988.1:p.Asn64Ile
NM_001376060.1:c.191A>T	NP_001362989.1:p.Asn64Ile
NM_001376061.1:c.191A>T	NP_001362990.1:p.Asn64Ile
NR_164757.1:n.851-427A>T