Canonical Allele Identifier: CA1327165474
Gene: ABCA12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214991105T= , CM000664.2:g.214991105T= GRCh38
NC_000002.11:g.215855829T= , CM000664.1:g.215855829T= GRCh37
NC_000002.10:g.215564074T= NCBI36
NG_007074.1:g.152323A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272895.12:c.3295-74A= MANE Select ENSP00000272895.7:n.3295-74A=
ENST00000272895.11:c.3295-74A= ENSP00000272895.7:n.3295-74A=
ENST00000389661.4:c.2341-74A= ENSP00000374312.4:n.2341-74A=
NM_015657.3:c.2341-74A= NP_056472.2:n.2341-74A=
NM_173076.2:c.3295-74A= NP_775099.2:n.3295-74A=
NR_103740.1:n.3595-74A=
XM_011510951.1:c.3295-74A= XP_011509253.1:n.3295-74A=
XM_011510952.1:c.3295-74A= XP_011509254.1:n.3295-74A=
XM_011510951.2:c.3295-74A= XP_011509253.1:n.3295-74A=
NM_173076.3:c.3295-74A= MANE Select NP_775099.2:n.3295-74A=
NR_103740.2:n.3793-74A=
NM_015657.4:c.2341-74A= NP_056472.2:n.2341-74A=