Canonical Allele Identifier: CA344235951

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097462G>C (hg19) ; chr1:g.202128334G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128334G>C , CM000663.2:g.202128334G>C	GRCh38
NC_000001.10:g.202097462G>C , CM000663.1:g.202097462G>C	GRCh37
NC_000001.9:g.200364085G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.805G>C
ENST00000682545.1:c.*230G>C	ENSP00000508402.1:n.*230G>C
ENST00000682887.1:c.1625G>C	ENSP00000506946.1:n.1625G>C
ENST00000683302.1:c.1155G>C	ENSP00000507885.1:p.Lys385Asn
ENST00000683557.1:c.*56G>C	ENSP00000508029.1:n.*56G>C
ENST00000367282.6:c.1224G>C MANE Select	ENSP00000356251.4:p.Lys408Asn
ENST00000367282.5:c.1224G>C	ENSP00000356251.4:p.Lys408Asn
NM_004767.3:c.1224G>C	NP_004758.3:p.Lys408Asn
XM_011510158.1:c.663G>C	XP_011508460.1:p.Lys221Asn
NM_004767.4:c.1224G>C	NP_004758.3:p.Lys408Asn
XM_011510158.2:c.663G>C	XP_011508460.1:p.Lys221Asn
NM_004767.5:c.1224G>C MANE Select	NP_004758.3:p.Lys408Asn