Canonical Allele Identifier: CA2581470328

Gene: DAP

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10752203C>G , CM000667.2:g.10752203C>G	GRCh38
NC_000005.9:g.10752315C>G , CM000667.1:g.10752315C>G	GRCh37
NC_000005.8:g.10805315C>G	NCBI36
NG_011546.1:g.14073G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230895.11:c.56-3932G>C MANE Select	ENSP00000230895.7:n.56-3932G>C
ENST00000230895.10:c.56-3932G>C	ENSP00000230895.6:n.56-3932G>C
ENST00000432074.2:c.56-3932G>C	ENSP00000394163.2:n.56-3932G>C
ENST00000508253.5:n.213-3932G>C
ENST00000508646.1:n.89-3932G>C
ENST00000510546.1:n.187-3932G>C
ENST00000514882.5:n.124-3932G>C
NM_001291963.1:c.56-3932G>C	NP_001278892.1:n.56-3932G>C
NM_004394.2:c.56-3932G>C	NP_004385.1:n.56-3932G>C
NM_001291963.2:c.56-3932G>C	NP_001278892.1:n.56-3932G>C
NM_004394.3:c.56-3932G>C MANE Select	NP_004385.1:n.56-3932G>C