Canonical Allele Identifier: CA794017885

Gene: MSANTD1

Linked Data

• dbSNP Id: rs1295632370
• gnomAD v3: 4-3256599-ACCTGTTCACATGCACAGC-A
• gnomAD v4: 4-3256599-ACCTGTTCACATGCACAGC-A
• MyVariant Identifiers: chr4:g.3258327_3258344del (hg19) ; chr4:g.3256600_3256617del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.3256606_3256623del , CM000666.2:g.3256606_3256623del	GRCh38
NC_000004.11:g.3258333_3258350del , CM000666.1:g.3258333_3258350del	GRCh37
NC_000004.10:g.3228131_3228148del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000505599.5:c.729+749_729+766del	ENSP00000425405.1:n.729+749_729+766del
ENST00000510580.1:c.765+713_765+730del	ENSP00000420966.1:n.765+713_765+730del
XM_011513464.1:c.729+749_729+766del	XP_011511766.1:n.729+749_729+766del
XR_924950.1:n.753+749_753+766del