Canonical Allele Identifier: CA2669711023

Gene: MSANTD1

Linked Data

• gnomAD v4: 4-3256400-GCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.3256401_3256402del , CM000666.2:g.3256401_3256402del	GRCh38
NC_000004.11:g.3258128_3258129del , CM000666.1:g.3258128_3258129del	GRCh37
NC_000004.10:g.3227926_3227927del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438480.7:c.*436_*437del MANE Select	ENSP00000411584.2:n.*436_*437del
ENST00000505599.5:c.729+544_729+545del	ENSP00000425405.1:n.729+544_729+545del
ENST00000507492.5:c.*436_*437del	ENSP00000423547.1:n.*436_*437del
ENST00000510580.1:c.765+508_765+509del	ENSP00000420966.1:n.765+508_765+509del
NM_001042690.1:c.*436_*437del	NP_001036155.1:n.*436_*437del
XM_006713883.2:c.*436_*437del	XP_006713946.1:n.*436_*437del
XM_011513464.1:c.729+544_729+545del	XP_011511766.1:n.729+544_729+545del
XM_011513465.1:c.*436_*437del	XP_011511767.1:n.*436_*437del
XM_011513466.1:c.*436_*437del	XP_011511768.1:n.*436_*437del
XM_011513467.1:c.*436_*437del	XP_011511769.1:n.*436_*437del
XR_924950.1:n.753+544_753+545del
NM_001330620.1:c.*436_*437del	NP_001317549.1:n.*436_*437del
XM_011513466.3:c.*436_*437del	XP_011511768.1:n.*436_*437del
XM_011513467.3:c.*436_*437del	XP_011511769.1:n.*436_*437del
NM_001042690.2:c.*436_*437del MANE Select	NP_001036155.1:n.*436_*437del
NM_001330620.2:c.*436_*437del	NP_001317549.1:n.*436_*437del