Canonical Allele Identifier: CA2091093
Community Standard Title: NM_173076.3(ABCA12):c.5848C>T (p.Arg1950Ter)
Gene: ABCA12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214966884G>A , CM000664.2:g.214966884G>A GRCh38
NC_000002.11:g.215831608G>A , CM000664.1:g.215831608G>A GRCh37
NC_000002.10:g.215539853G>A NCBI36
NG_007074.1:g.176544C>T

Transcript Alleles

HGVS Amino-acid Change
NM_173076.3:c.5848C>T MANE Select NP_775099.2:p.Arg1950Ter
ENST00000272895.12:c.5848C>T MANE Select ENSP00000272895.7:p.Arg1950Ter
NM_015657.3:c.4894C>T NP_056472.2:p.Arg1632Ter
NM_015657.4:c.4894C>T NP_056472.2:p.Arg1632Ter
NM_173076.2:c.5848C>T NP_775099.2:p.Arg1950Ter
NR_103740.1:n.6148C>T
NR_103740.2:n.6346C>T
ENST00000272895.11:c.5848C>T ENSP00000272895.7:p.Arg1950Ter
ENST00000389661.4:c.4894C>T ENSP00000374312.4:p.Arg1632Ter
XM_011510951.1:c.5857C>T XP_011509253.1:p.Arg1953Ter
XM_011510951.2:c.5857C>T XP_011509253.1:p.Arg1953Ter
XM_011510952.1:c.5857C>T XP_011509254.1:p.Arg1953Ter