Canonical Allele Identifier: CA350483388
Gene: ABCA12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215011443A>T , CM000664.2:g.215011443A>T GRCh38
NC_000002.11:g.215876167A>T , CM000664.1:g.215876167A>T GRCh37
NC_000002.10:g.215584412A>T NCBI36
NG_007074.1:g.131985T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.2328T>A MANE Select ENSP00000272895.7:p.Asn776Lys
ENST00000272895.11:c.2328T>A ENSP00000272895.7:p.Asn776Lys
ENST00000389661.4:c.1374T>A ENSP00000374312.4:p.Asn458Lys
NM_015657.3:c.1374T>A NP_056472.2:p.Asn458Lys
NM_173076.2:c.2328T>A NP_775099.2:p.Asn776Lys
NR_103740.1:n.2572T>A
XM_011510951.1:c.2328T>A XP_011509253.1:p.Asn776Lys
XM_011510952.1:c.2328T>A XP_011509254.1:p.Asn776Lys
XM_011510951.2:c.2328T>A XP_011509253.1:p.Asn776Lys
NM_173076.3:c.2328T>A MANE Select NP_775099.2:p.Asn776Lys
NR_103740.2:n.2770T>A
NM_015657.4:c.1374T>A NP_056472.2:p.Asn458Lys