Canonical Allele Identifier: CA338622380

Gene: EPHA2

Linked Data

• MyVariant Identifiers: chr1:g.16458637G>T (hg19) ; chr1:g.16132142G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16132142G>T , CM000663.2:g.16132142G>T	GRCh38
NC_000001.10:g.16458637G>T , CM000663.1:g.16458637G>T	GRCh37
NC_000001.9:g.16331224G>T	NCBI36
NG_021396.1:g.28946C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358432.8:c.2247C>A MANE Select	ENSP00000351209.5:p.Ser749Arg
ENST00000358432.7:c.2247C>A	ENSP00000351209.5:p.Ser749Arg
NM_004431.3:c.2247C>A	NP_004422.2:p.Ser749Arg
NM_001329090.1:c.2085C>A	NP_001316019.1:p.Ser695Arg
NM_004431.4:c.2247C>A	NP_004422.2:p.Ser749Arg
NM_004431.5:c.2247C>A MANE Select	NP_004422.2:p.Ser749Arg
NM_001329090.2:c.2085C>A	NP_001316019.1:p.Ser695Arg