Canonical Allele Identifier: CA1104180207
Gene: STEAP4 HGNC NCBI

Linked Data

dbSNP Id: rs1852953836
gnomAD v3: 7-88297956-C-A
gnomAD v4: 7-88297956-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.88297956C>A , CM000669.2:g.88297956C>A GRCh38
NC_000007.13:g.87927271C>A , CM000669.1:g.87927271C>A GRCh37
NC_000007.12:g.87765207C>A NCBI36
NG_028313.1:g.13958G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000380079.9:c.-3+8836G>T MANE Select ENSP00000369419.4:n.-3+8836G>T
ENST00000301959.9:c.-3+8836G>T ENSP00000305545.5:n.-3+8836G>T
ENST00000380079.8:c.-3+8836G>T ENSP00000369419.4:n.-3+8836G>T
ENST00000414498.1:c.-101-6942G>T ENSP00000394399.1:n.-101-6942G>T
NM_001205315.1:c.-101-6942G>T NP_001192244.1:n.-101-6942G>T
NM_001205316.1:c.-3+8836G>T NP_001192245.1:n.-3+8836G>T
NM_024636.3:c.-3+8836G>T NP_078912.2:n.-3+8836G>T
NM_001205315.2:c.-101-6942G>T NP_001192244.1:n.-101-6942G>T
NM_001205316.2:c.-3+8836G>T NP_001192245.1:n.-3+8836G>T
NM_024636.4:c.-3+8836G>T MANE Select NP_078912.2:n.-3+8836G>T