Canonical Allele Identifier: CA1723965490
Gene: STEAP4 HGNC NCBI

Linked Data

dbSNP Id: rs1852952585

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.88297900T>G , CM000669.2:g.88297900T>G GRCh38
NC_000007.13:g.87927215T>G , CM000669.1:g.87927215T>G GRCh37
NC_000007.12:g.87765151T>G NCBI36
NG_028313.1:g.14014A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000380079.9:c.-3+8892A>C MANE Select ENSP00000369419.4:n.-3+8892A>C
ENST00000301959.9:c.-3+8892A>C ENSP00000305545.5:n.-3+8892A>C
ENST00000380079.8:c.-3+8892A>C ENSP00000369419.4:n.-3+8892A>C
ENST00000414498.1:c.-101-6886A>C ENSP00000394399.1:n.-101-6886A>C
NM_001205315.1:c.-101-6886A>C NP_001192244.1:n.-101-6886A>C
NM_001205316.1:c.-3+8892A>C NP_001192245.1:n.-3+8892A>C
NM_024636.3:c.-3+8892A>C NP_078912.2:n.-3+8892A>C
NM_001205315.2:c.-101-6886A>C NP_001192244.1:n.-101-6886A>C
NM_001205316.2:c.-3+8892A>C NP_001192245.1:n.-3+8892A>C
NM_024636.4:c.-3+8892A>C MANE Select NP_078912.2:n.-3+8892A>C