Canonical Allele Identifier: CA393164003

Gene: CYP1A1

Linked Data

• MyVariant Identifiers: chr15:g.75012937C>G (hg19) ; chr15:g.74720596C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720596C>G , CM000677.2:g.74720596C>G	GRCh38
NC_000015.9:g.75012937C>G , CM000677.1:g.75012937C>G	GRCh37
NC_000015.8:g.72799990C>G	NCBI36
NG_008431.1:g.3055C>G
NG_008431.2:g.3055C>G
NG_061374.1:g.9933G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1432G>C MANE Select	ENSP00000369050.3:p.Val478Leu
ENST00000379727.7:c.1432G>C	ENSP00000369050.3:p.Val478Leu
ENST00000395048.6:c.1432G>C	ENSP00000378488.2:p.Val478Leu
ENST00000395049.8:c.1345G>C	ENSP00000378489.4:p.Val449Leu
ENST00000567032.5:c.1432G>C	ENSP00000456585.1:p.Val478Leu
ENST00000612821.4:c.1348G>C	ENSP00000479744.1:p.Val450Leu
ENST00000617691.4:c.1345G>C	ENSP00000482863.1:p.Val449Leu
NM_000499.3:c.1432G>C	NP_000490.1:p.Val478Leu
XM_005254185.1:c.1432G>C	XP_005254242.1:p.Val478Leu
NM_000499.5:c.1432G>C	NP_000490.1:p.Val478Leu
NM_001319216.2:c.1345G>C	NP_001306145.1:p.Val449Leu
NM_001319217.2:c.1432G>C MANE Select	NP_001306146.1:p.Val478Leu