Canonical Allele Identifier: CA2629504804
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754651_74754652insA , CM000677.2:g.74754651_74754652insA GRCh38
NC_000015.9:g.75046992_75046993insA , CM000677.1:g.75046992_75046993insA GRCh37
NC_000015.8:g.72834045_72834046insA NCBI36
NG_008431.1:g.37110_37111insA
NG_008431.2:g.37110_37111insA
NG_061543.1:g.10807_10808insA

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1254-140_1254-139insA MANE Select ENSP00000342007.4:n.1254-140_1254-139insA...
ENST00000343932.4:c.1254-140_1254-139insA ENSP00000342007.4:n.1254-140_1254-139insA...
NM_000761.4:c.1254-140_1254-139insA NP_000752.2:n.1254-140_1254-139insA
NM_000761.5:c.1254-140_1254-139insA MANE Select NP_000752.2:n.1254-140_1254-139insA