Canonical Allele Identifier: CA1327177477

Gene: ABCA12

Linked Data

• dbSNP Id: rs1700577728

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215019504G>C , CM000664.2:g.215019504G>C	GRCh38
NC_000002.11:g.215884228G>C , CM000664.1:g.215884228G>C	GRCh37
NC_000002.10:g.215592473G>C	NCBI36
NG_007074.1:g.123924C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.1544+36C>G MANE Select	ENSP00000272895.7:n.1544+36C>G
ENST00000272895.11:c.1544+36C>G	ENSP00000272895.7:n.1544+36C>G
ENST00000389661.4:c.590+36C>G	ENSP00000374312.4:n.590+36C>G
NM_015657.3:c.590+36C>G	NP_056472.2:n.590+36C>G
NM_173076.2:c.1544+36C>G	NP_775099.2:n.1544+36C>G
NR_103740.1:n.1788+36C>G
XM_011510951.1:c.1544+36C>G	XP_011509253.1:n.1544+36C>G
XM_011510952.1:c.1544+36C>G	XP_011509254.1:n.1544+36C>G
XM_011510951.2:c.1544+36C>G	XP_011509253.1:n.1544+36C>G
NM_173076.3:c.1544+36C>G MANE Select	NP_775099.2:n.1544+36C>G
NR_103740.2:n.1986+36C>G
NM_015657.4:c.590+36C>G	NP_056472.2:n.590+36C>G