Canonical Allele Identifier: CA1367078158

Gene: HESX1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.57199842A= , CM000665.2:g.57199842A=	GRCh38
NC_000003.11:g.57233870A= , CM000665.1:g.57233870A=	GRCh37
NC_000003.10:g.57208910A=	NCBI36
NG_008242.1:g.5411T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295934.8:c.77T= MANE Select	ENSP00000295934.3:p.Ile26=
ENST00000647958.1:c.77T=	ENSP00000498190.1:p.Ile26=
ENST00000295934.7:c.77T=	ENSP00000295934.3:p.Ile26=
ENST00000473921.2:c.77T=	ENSP00000418918.1:p.Ile26=
ENST00000495160.2:c.77T=	ENSP00000419615.2:p.Ile26=
NM_003865.2:c.77T=	NP_003856.1:p.Ile26=
XM_005265526.3:c.77T=	XP_005265583.1:p.Ile26=
XM_006713379.2:c.77T=	XP_006713442.1:p.Ile26=
XM_011534204.1:c.77T=	XP_011532506.1:p.Ile26=
XM_011534205.1:c.77T=	XP_011532507.1:p.Ile26=
XM_005265526.4:c.77T=	XP_005265583.1:p.Ile26=
XM_011534204.2:c.77T=	XP_011532506.1:p.Ile26=
XM_011534205.2:c.77T=	XP_011532507.1:p.Ile26=
XM_017007421.1:c.77T=	XP_016862910.1:p.Ile26=
XM_024453809.1:c.77T=	XP_024309577.1:p.Ile26=
NM_003865.3:c.77T= MANE Select	NP_003856.1:p.Ile26=
NM_001376058.1:c.77T=	NP_001362987.1:p.Ile26=
NM_001376059.1:c.77T=	NP_001362988.1:p.Ile26=
NM_001376060.1:c.77T=	NP_001362989.1:p.Ile26=
NM_001376061.1:c.77T=	NP_001362990.1:p.Ile26=
NR_164757.1:n.851-1350T=