Canonical Allele Identifier: CA2577235393
Gene: ABCA12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215019479C>A , CM000664.2:g.215019479C>A GRCh38
NC_000002.11:g.215884203C>A , CM000664.1:g.215884203C>A GRCh37
NC_000002.10:g.215592448C>A NCBI36
NG_007074.1:g.123949G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000272895.12:c.1545-31G>T MANE Select ENSP00000272895.7:n.1545-31G>T
ENST00000272895.11:c.1545-31G>T ENSP00000272895.7:n.1545-31G>T
ENST00000389661.4:c.591-31G>T ENSP00000374312.4:n.591-31G>T
NM_015657.3:c.591-31G>T NP_056472.2:n.591-31G>T
NM_173076.2:c.1545-31G>T NP_775099.2:n.1545-31G>T
NR_103740.1:n.1789-31G>T
XM_011510951.1:c.1545-31G>T XP_011509253.1:n.1545-31G>T
XM_011510952.1:c.1545-31G>T XP_011509254.1:n.1545-31G>T
XM_011510951.2:c.1545-31G>T XP_011509253.1:n.1545-31G>T
NM_173076.3:c.1545-31G>T MANE Select NP_775099.2:n.1545-31G>T
NR_103740.2:n.1987-31G>T
NM_015657.4:c.591-31G>T NP_056472.2:n.591-31G>T