Canonical Allele Identifier: CA2101050883
Gene: DACH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.71771373C>A , CM000675.2:g.71771373C>A GRCh38
NC_000013.10:g.72345505C>A , CM000675.1:g.72345505C>A GRCh37
NC_000013.9:g.71243506C>A NCBI36
NG_011849.3:g.100820G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000619232.2:c.849-89463G>T ENSP00000482797.1:n.849-89463G>T
ENST00000706274.1:c.392-89463G>T
ENST00000613252.5:c.849-89463G>T MANE Select ENSP00000482245.1:n.849-89463G>T
ENST00000611519.4:c.849-89463G>T ENSP00000482493.1:n.849-89463G>T
ENST00000613252.4:c.849-89463G>T ENSP00000482245.1:n.849-89463G>T
ENST00000619232.1:c.849-89463G>T ENSP00000482797.1:n.849-89463G>T
ENST00000620444.4:c.849-89463G>T ENSP00000481551.1:n.849-89463G>T
NM_004392.6:c.849-89463G>T NP_004383.4:n.849-89463G>T
NM_080759.5:c.849-89463G>T NP_542937.3:n.849-89463G>T
NM_080760.5:c.849-89463G>T NP_542938.3:n.849-89463G>T
XM_011534939.1:c.849-89463G>T XP_011533241.1:n.849-89463G>T
XM_011534940.1:c.849-89463G>T XP_011533242.1:n.849-89463G>T
XM_011534941.1:c.849-89463G>T XP_011533243.1:n.849-89463G>T
NM_001366712.1:c.849-89463G>T NP_001353641.1:n.849-89463G>T
XM_011534940.2:c.849-89463G>T XP_011533242.1:n.849-89463G>T
XM_011534941.2:c.849-89463G>T XP_011533243.1:n.849-89463G>T
NM_080759.6:c.849-89463G>T MANE Select NP_542937.3:n.849-89463G>T
NM_004392.7:c.849-89463G>T NP_004383.4:n.849-89463G>T
NM_080760.6:c.849-89463G>T NP_542938.3:n.849-89463G>T