Canonical Allele Identifier: CA3013639165

Gene: MSANTD1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.3256547C>T , CM000666.2:g.3256547C>T	GRCh38
NC_000004.11:g.3258274C>T , CM000666.1:g.3258274C>T	GRCh37
NC_000004.10:g.3228072C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438480.7:c.*582C>T MANE Select	ENSP00000411584.2:n.*582C>T
ENST00000505599.5:c.729+690C>T	ENSP00000425405.1:n.729+690C>T
ENST00000507492.5:c.*582C>T	ENSP00000423547.1:n.*582C>T
ENST00000510580.1:c.765+654C>T	ENSP00000420966.1:n.765+654C>T
NM_001042690.1:c.*582C>T	NP_001036155.1:n.*582C>T
XM_006713883.2:c.*582C>T	XP_006713946.1:n.*582C>T
XM_011513464.1:c.729+690C>T	XP_011511766.1:n.729+690C>T
XM_011513465.1:c.*582C>T	XP_011511767.1:n.*582C>T
XM_011513466.1:c.*582C>T	XP_011511768.1:n.*582C>T
XM_011513467.1:c.*582C>T	XP_011511769.1:n.*582C>T
XR_924950.1:n.753+690C>T
NM_001330620.1:c.*582C>T	NP_001317549.1:n.*582C>T
XM_011513466.3:c.*582C>T	XP_011511768.1:n.*582C>T
XM_011513467.3:c.*582C>T	XP_011511769.1:n.*582C>T
NM_001042690.2:c.*582C>T MANE Select	NP_001036155.1:n.*582C>T
NM_001330620.2:c.*582C>T	NP_001317549.1:n.*582C>T