Canonical Allele Identifier: CA2662978500

Gene: ABCA12

Linked Data

• gnomAD v4: 2-214980680-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214980680G>C , CM000664.2:g.214980680G>C	GRCh38
NC_000002.11:g.215845404G>C , CM000664.1:g.215845404G>C	GRCh37
NC_000002.10:g.215553649G>C	NCBI36
NG_007074.1:g.162748C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.4580-37C>G MANE Select	ENSP00000272895.7:n.4580-37C>G
ENST00000272895.11:c.4580-37C>G	ENSP00000272895.7:n.4580-37C>G
ENST00000389661.4:c.3626-37C>G	ENSP00000374312.4:n.3626-37C>G
NM_015657.3:c.3626-37C>G	NP_056472.2:n.3626-37C>G
NM_173076.2:c.4580-37C>G	NP_775099.2:n.4580-37C>G
NR_103740.1:n.4880-37C>G
XM_011510951.1:c.4589-37C>G	XP_011509253.1:n.4589-37C>G
XM_011510952.1:c.4589-37C>G	XP_011509254.1:n.4589-37C>G
XM_011510951.2:c.4589-37C>G	XP_011509253.1:n.4589-37C>G
NM_173076.3:c.4580-37C>G MANE Select	NP_775099.2:n.4580-37C>G
NR_103740.2:n.5078-37C>G
NM_015657.4:c.3626-37C>G	NP_056472.2:n.3626-37C>G