Canonical Allele Identifier: CA613904721

Gene: PTGER2

Linked Data

• dbSNP Id: rs1400519146
• gnomAD v2: 14-52789139-ACAAAGATCACAAGGCAAAGGGCAAAAG-A
• gnomAD v3: 14-52322421-ACAAAGATCACAAGGCAAAGGGCAAAAG-A
• gnomAD v4: 14-52322421-ACAAAGATCACAAGGCAAAGGGCAAAAG-A
• MyVariant Identifiers: chr14:g.52789140_52789166del (hg19) ; chr14:g.52322422_52322448del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.52322451_52322477del , CM000676.2:g.52322451_52322477del	GRCh38
NC_000014.8:g.52789169_52789195del , CM000676.1:g.52789169_52789195del	GRCh37
NC_000014.7:g.51858919_51858945del	NCBI36
NG_013082.1:g.13154_13180del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245457.6:c.844-4770_844-4744del MANE Select	ENSP00000245457.5:n.844-4770_844-4744del
ENST00000245457.5:c.844-4770_844-4744del	ENSP00000245457.5:n.844-4770_844-4744del
ENST00000557436.1:c.79-4770_79-4744del	ENSP00000450933.1:n.79-4770_79-4744del
NM_000956.3:c.844-4770_844-4744del	NP_000947.2:n.844-4770_844-4744del
NM_000956.4:c.844-4770_844-4744del MANE Select	NP_000947.2:n.844-4770_844-4744del