Canonical Allele Identifier: CA2581401952

Gene: MSANTD1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.3256594G>C , CM000666.2:g.3256594G>C	GRCh38
NC_000004.11:g.3258321G>C , CM000666.1:g.3258321G>C	GRCh37
NC_000004.10:g.3228119G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000438480.7:c.*629G>C MANE Select	ENSP00000411584.2:n.*629G>C
ENST00000505599.5:c.729+737G>C	ENSP00000425405.1:n.729+737G>C
ENST00000507492.5:c.*629G>C	ENSP00000423547.1:n.*629G>C
ENST00000510580.1:c.765+701G>C	ENSP00000420966.1:n.765+701G>C
NM_001042690.1:c.*629G>C	NP_001036155.1:n.*629G>C
XM_006713883.2:c.*629G>C	XP_006713946.1:n.*629G>C
XM_011513464.1:c.729+737G>C	XP_011511766.1:n.729+737G>C
XM_011513465.1:c.*629G>C	XP_011511767.1:n.*629G>C
XM_011513466.1:c.*629G>C	XP_011511768.1:n.*629G>C
XM_011513467.1:c.*629G>C	XP_011511769.1:n.*629G>C
XR_924950.1:n.753+737G>C
NM_001330620.1:c.*629G>C	NP_001317549.1:n.*629G>C
XM_011513466.3:c.*629G>C	XP_011511768.1:n.*629G>C
XM_011513467.3:c.*629G>C	XP_011511769.1:n.*629G>C
NM_001042690.2:c.*629G>C MANE Select	NP_001036155.1:n.*629G>C
NM_001330620.2:c.*629G>C	NP_001317549.1:n.*629G>C