Canonical Allele Identifier: CA1723965647
Gene: STEAP4 HGNC NCBI

Linked Data

dbSNP Id: rs1852959643

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.88298178A>G , CM000669.2:g.88298178A>G GRCh38
NC_000007.13:g.87927493A>G , CM000669.1:g.87927493A>G GRCh37
NC_000007.12:g.87765429A>G NCBI36
NG_028313.1:g.13736T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000380079.9:c.-3+8614T>C MANE Select ENSP00000369419.4:n.-3+8614T>C
ENST00000301959.9:c.-3+8614T>C ENSP00000305545.5:n.-3+8614T>C
ENST00000380079.8:c.-3+8614T>C ENSP00000369419.4:n.-3+8614T>C
ENST00000414498.1:c.-101-7164T>C ENSP00000394399.1:n.-101-7164T>C
NM_001205315.1:c.-101-7164T>C NP_001192244.1:n.-101-7164T>C
NM_001205316.1:c.-3+8614T>C NP_001192245.1:n.-3+8614T>C
NM_024636.3:c.-3+8614T>C NP_078912.2:n.-3+8614T>C
NM_001205315.2:c.-101-7164T>C NP_001192244.1:n.-101-7164T>C
NM_001205316.2:c.-3+8614T>C NP_001192245.1:n.-3+8614T>C
NM_024636.4:c.-3+8614T>C MANE Select NP_078912.2:n.-3+8614T>C