Canonical Allele Identifier: CA487828355

Gene: GPR68

Linked Data

• MyVariant Identifiers: chr14:g.91700855T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91234511T>C , CM000676.2:g.91234511T>C	GRCh38
NC_000014.8:g.91700855T>C , CM000676.1:g.91700855T>C	GRCh37
NC_000014.7:g.90770608T>C	NCBI36
NG_052988.1:g.24370A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650645.1:c.540A>G MANE Select	ENSP00000498702.1:p.Ala180=
ENST00000529102.1:c.540A>G	ENSP00000432740.1:p.Ala180=
ENST00000531499.2:c.540A>G	ENSP00000434045.2:p.Ala180=
ENST00000535815.5:c.540A>G	ENSP00000440797.1:p.Ala180=
NM_001177676.1:c.540A>G	NP_001171147.1:p.Ala180=
NM_003485.3:c.540A>G	NP_003476.3:p.Ala180=
XM_005268110.3:c.570A>G	XP_005268167.1:p.Ala190=
XM_005268111.2:c.570A>G	XP_005268168.1:p.Ala190=
XM_005268112.2:c.570A>G	XP_005268169.1:p.Ala190=
XM_006720262.2:c.570A>G	XP_006720325.1:p.Ala190=
XM_011537196.1:c.570A>G	XP_011535498.1:p.Ala190=
XM_011537197.1:c.570A>G	XP_011535499.1:p.Ala190=
XM_011537198.1:c.570A>G	XP_011535500.1:p.Ala190=
XM_011537199.1:c.570A>G	XP_011535501.1:p.Ala190=
XM_011537200.1:c.570A>G	XP_011535502.1:p.Ala190=
NM_001348437.1:c.540A>G	NP_001335366.1:p.Ala180=
XM_005268110.4:c.570A>G	XP_005268167.1:p.Ala190=
XM_005268111.3:c.570A>G	XP_005268168.1:p.Ala190=
XM_005268112.3:c.570A>G	XP_005268169.1:p.Ala190=
XM_006720262.3:c.570A>G	XP_006720325.1:p.Ala190=
XM_011537196.2:c.570A>G	XP_011535498.1:p.Ala190=
XM_011537197.3:c.570A>G	XP_011535499.1:p.Ala190=
XM_011537198.2:c.570A>G	XP_011535500.1:p.Ala190=
XM_011537199.2:c.570A>G	XP_011535501.1:p.Ala190=
NM_001177676.2:c.540A>G MANE Select	NP_001171147.1:p.Ala180=