Canonical Allele Identifier: CA1723965629
Gene: STEAP4 HGNC NCBI

Linked Data

dbSNP Id: rs1852958616

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.88298140G>C , CM000669.2:g.88298140G>C GRCh38
NC_000007.13:g.87927455G>C , CM000669.1:g.87927455G>C GRCh37
NC_000007.12:g.87765391G>C NCBI36
NG_028313.1:g.13774C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000380079.9:c.-3+8652C>G MANE Select ENSP00000369419.4:n.-3+8652C>G
ENST00000301959.9:c.-3+8652C>G ENSP00000305545.5:n.-3+8652C>G
ENST00000380079.8:c.-3+8652C>G ENSP00000369419.4:n.-3+8652C>G
ENST00000414498.1:c.-101-7126C>G ENSP00000394399.1:n.-101-7126C>G
NM_001205315.1:c.-101-7126C>G NP_001192244.1:n.-101-7126C>G
NM_001205316.1:c.-3+8652C>G NP_001192245.1:n.-3+8652C>G
NM_024636.3:c.-3+8652C>G NP_078912.2:n.-3+8652C>G
NM_001205315.2:c.-101-7126C>G NP_001192244.1:n.-101-7126C>G
NM_001205316.2:c.-3+8652C>G NP_001192245.1:n.-3+8652C>G
NM_024636.4:c.-3+8652C>G MANE Select NP_078912.2:n.-3+8652C>G