Canonical Allele Identifier: CA13279466
Gene: SYCE1 HGNC NCBI
CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs10857748

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133558806T>C , CM000672.2:g.133558806T>C GRCh38
NC_000010.10:g.135372310T>C , CM000672.1:g.135372310T>C GRCh37
NC_000010.9:g.135222300T>C NCBI36
NG_052008.1:g.14470A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000343131.7:c.271+71A>G (SYCE1) MANE Select ENSP00000341282.5:n.271+71A>G
ENST00000303903.10:c.271+71A>G (SYCE1) ENSP00000303978.5:n.271+71A>G
ENST00000343131.5:c.271+71A>G (SYCE1) ENSP00000341282.5:n.271+71A>G
ENST00000368517.7:c.163+71A>G (SYCE1) ENSP00000357503.3:n.163+71A>G
ENST00000368520.1:n.5504T>C (CYP2E1)
ENST00000479535.2:n.1404+71A>G (SYCE1)
NM_001143763.1:c.271+71A>G (SYCE1) NP_001137235.1:n.271+71A>G
NM_001143764.1:c.271+71A>G (SYCE1) NP_001137236.1:n.271+71A>G
NM_130784.2:c.163+71A>G (SYCE1) NP_570140.1:n.163+71A>G
NM_001143764.2:c.271+71A>G (SYCE1) NP_001137236.1:n.271+71A>G
NM_130784.3:c.163+71A>G (SYCE1) NP_570140.1:n.163+71A>G
NM_001143764.3:c.271+71A>G (SYCE1) MANE Select NP_001137236.1:n.271+71A>G
NM_001143763.2:c.271+71A>G (SYCE1) NP_001137235.1:n.271+71A>G
NM_130784.4:c.163+71A>G (SYCE1) NP_570140.1:n.163+71A>G