Canonical Allele Identifier: CA1330219

Gene: GPR37L1

Linked Data

• dbSNP Id: rs751408912
• ExAC: 1:202097542 G / T
• gnomAD v2: 1-202097542-G-T
• gnomAD v3: 1-202128414-G-T
• gnomAD v4: 1-202128414-G-T
• MyVariant Identifiers: chr1:g.202097542G>T (hg19) ; chr1:g.202128414G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128414G>T , CM000663.2:g.202128414G>T	GRCh38
NC_000001.10:g.202097542G>T , CM000663.1:g.202097542G>T	GRCh37
NC_000001.9:g.200364165G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.885G>T
ENST00000682545.1:c.*310G>T	ENSP00000508402.1:n.*310G>T
ENST00000682887.1:c.1705G>T	ENSP00000506946.1:n.1705G>T
ENST00000683302.1:c.1235G>T	ENSP00000507885.1:p.Cys412Phe
ENST00000683557.1:c.*136G>T	ENSP00000508029.1:n.*136G>T
ENST00000367282.6:c.1304G>T MANE Select	ENSP00000356251.4:p.Cys435Phe
ENST00000367282.5:c.1304G>T	ENSP00000356251.4:p.Cys435Phe
NM_004767.3:c.1304G>T	NP_004758.3:p.Cys435Phe
XM_011510158.1:c.743G>T	XP_011508460.1:p.Cys248Phe
NM_004767.4:c.1304G>T	NP_004758.3:p.Cys435Phe
XM_011510158.2:c.743G>T	XP_011508460.1:p.Cys248Phe
NM_004767.5:c.1304G>T MANE Select	NP_004758.3:p.Cys435Phe