Canonical Allele Identifier: CA12482812
Community Standard Title: NM_001868.4(CPA1):c.148-140C>T
Gene: CPA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.130381490C>T , CM000669.2:g.130381490C>T GRCh38
NC_000007.13:g.130021331C>T , CM000669.1:g.130021331C>T GRCh37
NC_000007.12:g.129808567C>T NCBI36
NG_042276.1:g.6120C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001868.4:c.148-140C>T MANE Select NP_001859.1:n.148-140C>T
ENST00000011292.8:c.148-140C>T MANE Select ENSP00000011292.3:n.148-140C>T
NM_001868.3:c.148-140C>T NP_001859.1:n.148-140C>T
ENST00000011292.7:c.148-140C>T ENSP00000011292.3:n.148-140C>T
ENST00000476062.5:c.-117-140C>T ENSP00000419408.1:n.-117-140C>T
ENST00000481342.5:c.-117-140C>T ENSP00000420218.1:n.-117-140C>T
ENST00000484324.1:c.-117-140C>T ENSP00000419497.1:n.-117-140C>T
ENST00000491460.5:n.175-205C>T
ENST00000604896.5:c.141+344C>T ENSP00000475021.1:n.141+344C>T