Canonical Allele Identifier: CA1434130890

Gene: MSANTD1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.3256411C= , CM000666.2:g.3256411C=	GRCh38
NC_000004.11:g.3258138C= , CM000666.1:g.3258138C=	GRCh37
NC_000004.10:g.3227936C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438480.7:c.*446C= MANE Select	ENSP00000411584.2:n.*446C=
ENST00000505599.5:c.729+554C=	ENSP00000425405.1:n.729+554C=
ENST00000507492.5:c.*446C=	ENSP00000423547.1:n.*446C=
ENST00000510580.1:c.765+518C=	ENSP00000420966.1:n.765+518C=
NM_001042690.1:c.*446C=	NP_001036155.1:n.*446C=
XM_006713883.2:c.*446C=	XP_006713946.1:n.*446C=
XM_011513464.1:c.729+554C=	XP_011511766.1:n.729+554C=
XM_011513465.1:c.*446C=	XP_011511767.1:n.*446C=
XM_011513466.1:c.*446C=	XP_011511768.1:n.*446C=
XM_011513467.1:c.*446C=	XP_011511769.1:n.*446C=
XR_924950.1:n.753+554C=
NM_001330620.1:c.*446C=	NP_001317549.1:n.*446C=
XM_011513466.3:c.*446C=	XP_011511768.1:n.*446C=
XM_011513467.3:c.*446C=	XP_011511769.1:n.*446C=
NM_001042690.2:c.*446C= MANE Select	NP_001036155.1:n.*446C=
NM_001330620.2:c.*446C=	NP_001317549.1:n.*446C=