Canonical Allele Identifier: CA1527128606

Gene: DAP

Linked Data

• dbSNP Id: rs1739531344

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10733678A>C , CM000667.2:g.10733678A>C	GRCh38
NC_000005.9:g.10733790A>C , CM000667.1:g.10733790A>C	GRCh37
NC_000005.8:g.10786790A>C	NCBI36
NG_011546.1:g.32598T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230895.11:c.152+14497T>G MANE Select	ENSP00000230895.7:n.152+14497T>G
ENST00000230895.10:c.152+14497T>G	ENSP00000230895.6:n.152+14497T>G
ENST00000432074.2:c.152+14497T>G	ENSP00000394163.2:n.152+14497T>G
ENST00000508253.5:n.309+14497T>G
ENST00000514882.5:n.220+14497T>G
NM_001291963.1:c.152+14497T>G	NP_001278892.1:n.152+14497T>G
NM_004394.2:c.152+14497T>G	NP_004385.1:n.152+14497T>G
NM_001291963.2:c.152+14497T>G	NP_001278892.1:n.152+14497T>G
NM_004394.3:c.152+14497T>G MANE Select	NP_004385.1:n.152+14497T>G