Canonical Allele Identifier: CA1367090036

Gene: HESX1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.57198246G= , CM000665.2:g.57198246G=	GRCh38
NC_000003.11:g.57232274G= , CM000665.1:g.57232274G=	GRCh37
NC_000003.10:g.57207314G=	NCBI36
NG_008242.1:g.7007C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295934.8:c.509C= MANE Select	ENSP00000295934.3:p.Ser170=
ENST00000647958.1:c.509C=	ENSP00000498190.1:p.Ser170=
ENST00000295934.7:c.509C=	ENSP00000295934.3:p.Ser170=
ENST00000473921.2:c.407C=	ENSP00000418918.1:p.Ser136=
NM_003865.2:c.509C=	NP_003856.1:p.Ser170=
XM_005265526.3:c.509C=	XP_005265583.1:p.Ser170=
XM_006713379.2:c.509C=	XP_006713442.1:p.Ser170=
XM_011534204.1:c.509C=	XP_011532506.1:p.Ser170=
XM_011534205.1:c.509C=	XP_011532507.1:p.Ser170=
XM_005265526.4:c.509C=	XP_005265583.1:p.Ser170=
XM_011534204.2:c.509C=	XP_011532506.1:p.Ser170=
XM_011534205.2:c.509C=	XP_011532507.1:p.Ser170=
XM_017007421.1:c.509C=	XP_016862910.1:p.Ser170=
XM_024453809.1:c.509C=	XP_024309577.1:p.Ser170=
NM_003865.3:c.509C= MANE Select	NP_003856.1:p.Ser170=
NM_001376058.1:c.509C=	NP_001362987.1:p.Ser170=
NM_001376059.1:c.509C=	NP_001362988.1:p.Ser170=
NM_001376060.1:c.509C=	NP_001362989.1:p.Ser170=
NM_001376061.1:c.509C=	NP_001362990.1:p.Ser170=
NR_164757.1:n.1002C=