Canonical Allele Identifier: CA1434130893

Gene: MSANTD1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.3256415_3256424delinsGGGAGCTCTC , CM000666.2:g.3256415_3256424delinsGGGAGCTCTC	GRCh38
NC_000004.11:g.3258142_3258151delinsGGGAGCTCTC , CM000666.1:g.3258142_3258151delinsGGGAGCTCTC	GRCh37
NC_000004.10:g.3227940_3227949delinsGGGAGCTCTC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438480.7:c.*450_*459delinsGGGAGCTCTC MANE Select	ENSP00000411584.2:n.*450_*459delinsGGGAGCTCTC
ENST00000505599.5:c.729+558_729+567delinsGGGAGCTCTC	ENSP00000425405.1:n.729+558_729+567delinsGGGAGCTCTC
ENST00000507492.5:c.*450_*459delinsGGGAGCTCTC	ENSP00000423547.1:n.*450_*459delinsGGGAGCTCTC
ENST00000510580.1:c.765+522_765+531delinsGGGAGCTCTC	ENSP00000420966.1:n.765+522_765+531delinsGGGAGCTCTC
NM_001042690.1:c.*450_*459delinsGGGAGCTCTC	NP_001036155.1:n.*450_*459delinsGGGAGCTCTC
XM_006713883.2:c.*450_*459delinsGGGAGCTCTC	XP_006713946.1:n.*450_*459delinsGGGAGCTCTC
XM_011513464.1:c.729+558_729+567delinsGGGAGCTCTC	XP_011511766.1:n.729+558_729+567delinsGGGAGCTCTC
XM_011513465.1:c.*450_*459delinsGGGAGCTCTC	XP_011511767.1:n.*450_*459delinsGGGAGCTCTC
XM_011513466.1:c.*450_*459delinsGGGAGCTCTC	XP_011511768.1:n.*450_*459delinsGGGAGCTCTC
XM_011513467.1:c.*450_*459delinsGGGAGCTCTC	XP_011511769.1:n.*450_*459delinsGGGAGCTCTC
XR_924950.1:n.753+558_753+567delinsGGGAGCTCTC
NM_001330620.1:c.*450_*459delinsGGGAGCTCTC	NP_001317549.1:n.*450_*459delinsGGGAGCTCTC
XM_011513466.3:c.*450_*459delinsGGGAGCTCTC	XP_011511768.1:n.*450_*459delinsGGGAGCTCTC
XM_011513467.3:c.*450_*459delinsGGGAGCTCTC	XP_011511769.1:n.*450_*459delinsGGGAGCTCTC
NM_001042690.2:c.*450_*459delinsGGGAGCTCTC MANE Select	NP_001036155.1:n.*450_*459delinsGGGAGCTCTC
NM_001330620.2:c.*450_*459delinsGGGAGCTCTC	NP_001317549.1:n.*450_*459delinsGGGAGCTCTC