Canonical Allele Identifier: CA203900677

Gene: MALRD1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.19640584T>C , CM000672.2:g.19640584T>C	GRCh38
NC_000010.10:g.19929513T>C , CM000672.1:g.19929513T>C	GRCh37
NC_000010.9:g.19969519T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454679.7:c.6137+24661T>C MANE Select	ENSP00000412763.3:n.6137+24661T>C
ENST00000377265.3:c.1188+24661T>C
ENST00000377266.7:c.4207+32682T>C	ENSP00000366477.3:n.4207+32682T>C
ENST00000454679.6:c.6137+24661T>C	ENSP00000412763.3:n.6137+24661T>C
NM_001142308.2:c.6137+24661T>C	NP_001135780.2:n.6137+24661T>C
XM_011519453.1:c.6197+24661T>C	XP_011517755.1:n.6197+24661T>C
XM_011519454.1:c.6116+24661T>C	XP_011517756.1:n.6116+24661T>C
XM_011519455.1:c.6023+24661T>C	XP_011517757.1:n.6023+24661T>C
XM_011519453.2:c.6197+24661T>C	XP_011517755.1:n.6197+24661T>C
XM_011519455.2:c.6023+24661T>C	XP_011517757.1:n.6023+24661T>C
XM_017016182.1:c.5924+24661T>C	XP_016871671.1:n.5924+24661T>C
XM_017016184.1:c.4397+24661T>C	XP_016871673.1:n.4397+24661T>C
XM_017016185.1:c.4397+24661T>C	XP_016871674.1:n.4397+24661T>C
XM_017016186.1:c.2939+24661T>C	XP_016871675.1:n.2939+24661T>C
XR_001747102.1:n.6841+24661T>C
NM_001142308.3:c.6137+24661T>C MANE Select	NP_001135780.2:n.6137+24661T>C