Canonical Allele Identifier: CA162520616

Gene: STEAP4

Linked Data

• dbSNP Id: rs899377642
• gnomAD v2: 7-87927467-C-A
• gnomAD v3: 7-88298152-C-A
• gnomAD v4: 7-88298152-C-A
• MyVariant Identifiers: chr7:g.87927467C>A (hg19) ; chr7:g.88298152C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.88298152C>A , CM000669.2:g.88298152C>A	GRCh38
NC_000007.13:g.87927467C>A , CM000669.1:g.87927467C>A	GRCh37
NC_000007.12:g.87765403C>A	NCBI36
NG_028313.1:g.13762G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000380079.9:c.-3+8640G>T MANE Select	ENSP00000369419.4:n.-3+8640G>T
ENST00000301959.9:c.-3+8640G>T	ENSP00000305545.5:n.-3+8640G>T
ENST00000380079.8:c.-3+8640G>T	ENSP00000369419.4:n.-3+8640G>T
ENST00000414498.1:c.-101-7138G>T	ENSP00000394399.1:n.-101-7138G>T
NM_001205315.1:c.-101-7138G>T	NP_001192244.1:n.-101-7138G>T
NM_001205316.1:c.-3+8640G>T	NP_001192245.1:n.-3+8640G>T
NM_024636.3:c.-3+8640G>T	NP_078912.2:n.-3+8640G>T
NM_001205315.2:c.-101-7138G>T	NP_001192244.1:n.-101-7138G>T
NM_001205316.2:c.-3+8640G>T	NP_001192245.1:n.-3+8640G>T
NM_024636.4:c.-3+8640G>T MANE Select	NP_078912.2:n.-3+8640G>T