Canonical Allele Identifier: CA2669711011

Gene: MSANTD1

Linked Data

• gnomAD v4: 4-3256392-GGGTTGGGGCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.3256395_3256404del , CM000666.2:g.3256395_3256404del	GRCh38
NC_000004.11:g.3258122_3258131del , CM000666.1:g.3258122_3258131del	GRCh37
NC_000004.10:g.3227920_3227929del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438480.7:c.*430_*439del MANE Select	ENSP00000411584.2:n.*430_*439del
ENST00000505599.5:c.729+538_729+547del	ENSP00000425405.1:n.729+538_729+547del
ENST00000507492.5:c.*430_*439del	ENSP00000423547.1:n.*430_*439del
ENST00000510580.1:c.765+502_765+511del	ENSP00000420966.1:n.765+502_765+511del
NM_001042690.1:c.*430_*439del	NP_001036155.1:n.*430_*439del
XM_006713883.2:c.*430_*439del	XP_006713946.1:n.*430_*439del
XM_011513464.1:c.729+538_729+547del	XP_011511766.1:n.729+538_729+547del
XM_011513465.1:c.*430_*439del	XP_011511767.1:n.*430_*439del
XM_011513466.1:c.*430_*439del	XP_011511768.1:n.*430_*439del
XM_011513467.1:c.*430_*439del	XP_011511769.1:n.*430_*439del
XR_924950.1:n.753+538_753+547del
NM_001330620.1:c.*430_*439del	NP_001317549.1:n.*430_*439del
XM_011513466.3:c.*430_*439del	XP_011511768.1:n.*430_*439del
XM_011513467.3:c.*430_*439del	XP_011511769.1:n.*430_*439del
NM_001042690.2:c.*430_*439del MANE Select	NP_001036155.1:n.*430_*439del
NM_001330620.2:c.*430_*439del	NP_001317549.1:n.*430_*439del