Canonical Allele Identifier: CA324270937

Gene: DMC1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38551830C>A , CM000684.2:g.38551830C>A	GRCh38
NC_000022.10:g.38947835C>A , CM000684.1:g.38947835C>A	GRCh37
NC_000022.9:g.37277781C>A	NCBI36
NG_017203.1:g.23355G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216024.7:c.421+836G>T MANE Select	ENSP00000216024.2:n.421+836G>T
ENST00000216024.6:c.421+836G>T	ENSP00000216024.2:n.421+836G>T
ENST00000428462.6:c.421+836G>T	ENSP00000412703.2:n.421+836G>T
ENST00000439567.5:c.421+836G>T	ENSP00000391385.1:n.421+836G>T
ENST00000478820.1:n.596+836G>T
ENST00000616615.4:c.421+836G>T	ENSP00000477737.1:n.421+836G>T
NM_001278208.1:c.421+836G>T	NP_001265137.1:n.421+836G>T
NM_007068.3:c.421+836G>T	NP_008999.2:n.421+836G>T
XM_006724112.2:c.421+836G>T	XP_006724175.1:n.421+836G>T
XM_011529834.1:c.421+836G>T	XP_011528136.1:n.421+836G>T
XM_011529835.1:c.421+836G>T	XP_011528137.1:n.421+836G>T
XM_011529836.1:c.380-1833G>T	XP_011528138.1:n.380-1833G>T
XM_011529837.1:c.421+836G>T	XP_011528139.1:n.421+836G>T
XM_011529838.1:c.379+3527G>T	XP_011528140.1:n.379+3527G>T
NM_001363017.1:c.421+836G>T	NP_001349946.1:n.421+836G>T
XM_011529834.2:c.421+836G>T	XP_011528136.1:n.421+836G>T
XM_011529835.2:c.421+836G>T	XP_011528137.1:n.421+836G>T
XM_011529837.2:c.421+836G>T	XP_011528139.1:n.421+836G>T
XM_017028542.2:c.379+3527G>T	XP_016884031.1:n.379+3527G>T
NM_007068.4:c.421+836G>T MANE Select	NP_008999.2:n.421+836G>T
NM_001363017.2:c.421+836G>T	NP_001349946.1:n.421+836G>T
NM_001278208.2:c.421+836G>T	NP_001265137.1:n.421+836G>T