Canonical Allele Identifier: CA319457727

Gene: EPCIP EPCIP-AS1

Linked Data

• dbSNP Id: rs2154427
• gnomAD v2: 21-34168573-G-A
• gnomAD v3: 21-32796263-G-A
• gnomAD v4: 21-32796263-G-A
• MyVariant Identifiers: chr21:g.34168573G>A (hg19) ; chr21:g.32796263G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.32796263G>A , CM000683.2:g.32796263G>A	GRCh38
NC_000021.8:g.34168573G>A , CM000683.1:g.34168573G>A	GRCh37
NC_000021.7:g.33090443G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000479548.2:c.-64-1778C>T (EPCIP) MANE Select	ENSP00000418653.1:n.-64-1778C>T
ENST00000382373.4:c.180-1880C>T (EPCIP)	ENSP00000371810.4:n.180-1880C>T
ENST00000479548.1:c.-64-1778C>T (EPCIP)	ENSP00000418653.1:n.-64-1778C>T
ENST00000487113.1:c.-64-1778C>T (EPCIP)	ENSP00000418511.1:n.-64-1778C>T
ENST00000490358.5:c.-64-1778C>T (EPCIP)	ENSP00000418830.1:n.-64-1778C>T
ENST00000536776.1:c.-64-1778C>T (EPCIP)	ENSP00000444950.1:n.-64-1778C>T
NM_001162495.2:c.-64-1778C>T (EPCIP)	NP_001155967.2:n.-64-1778C>T
NM_001162496.2:c.-64-1778C>T (EPCIP)	NP_001155968.2:n.-64-1778C>T
NM_019596.5:c.-64-1778C>T (EPCIP)	NP_062542.5:n.-64-1778C>T
NR_024622.1:n.435-676G>A (EPCIP-AS1)
NR_024623.1:n.423-676G>A (EPCIP-AS1)
XM_011529652.1:c.-64-1778C>T (EPCIP)	XP_011527954.1:n.-64-1778C>T
NM_001162495.3:c.-64-1778C>T (EPCIP) MANE Select	NP_001155967.2:n.-64-1778C>T
NM_001162496.3:c.-64-1778C>T (EPCIP)	NP_001155968.2:n.-64-1778C>T
NM_019596.6:c.-64-1778C>T (EPCIP)	NP_062542.5:n.-64-1778C>T