Canonical Allele Identifier: CA1434130918

Gene: MSANTD1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.3256443G= , CM000666.2:g.3256443G=	GRCh38
NC_000004.11:g.3258170G= , CM000666.1:g.3258170G=	GRCh37
NC_000004.10:g.3227968G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438480.7:c.*478G= MANE Select	ENSP00000411584.2:n.*478G=
ENST00000505599.5:c.729+586G=	ENSP00000425405.1:n.729+586G=
ENST00000507492.5:c.*478G=	ENSP00000423547.1:n.*478G=
ENST00000510580.1:c.765+550G=	ENSP00000420966.1:n.765+550G=
NM_001042690.1:c.*478G=	NP_001036155.1:n.*478G=
XM_006713883.2:c.*478G=	XP_006713946.1:n.*478G=
XM_011513464.1:c.729+586G=	XP_011511766.1:n.729+586G=
XM_011513465.1:c.*478G=	XP_011511767.1:n.*478G=
XM_011513466.1:c.*478G=	XP_011511768.1:n.*478G=
XM_011513467.1:c.*478G=	XP_011511769.1:n.*478G=
XR_924950.1:n.753+586G=
NM_001330620.1:c.*478G=	NP_001317549.1:n.*478G=
XM_011513466.3:c.*478G=	XP_011511768.1:n.*478G=
XM_011513467.3:c.*478G=	XP_011511769.1:n.*478G=
NM_001042690.2:c.*478G= MANE Select	NP_001036155.1:n.*478G=
NM_001330620.2:c.*478G=	NP_001317549.1:n.*478G=