Canonical Allele Identifier: CA465003989

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37428538C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428541C>T , CM000671.2:g.37428541C>T	GRCh38
NC_000009.11:g.37428538C>T , CM000671.1:g.37428538C>T	GRCh37
NC_000009.10:g.37418538C>T	NCBI36
NG_008135.1:g.10832C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.462C>T MANE Select	ENSP00000313432.6:p.Ser154=
ENST00000318158.10:c.462C>T	ENSP00000313432.6:p.Ser154=
ENST00000377824.8:n.499C>T
ENST00000460882.5:n.489C>T
ENST00000480596.5:n.4C>T
ENST00000491488.5:n.167C>T
ENST00000493368.5:n.519C>T
ENST00000497693.1:n.836C>T
ENST00000607784.1:c.462C>T	ENSP00000475569.1:p.Ser154=
NM_012203.1:c.462C>T	NP_036335.1:p.Ser154=
XM_005251631.1:c.141C>T	XP_005251688.1:p.Ser47=
XM_011518073.1:c.-301C>T	XP_011516375.1:n.-301C>T
XR_929374.1:n.547C>T
XM_017015320.2:c.462C>T	XP_016870809.1:p.Ser154=
XM_017015321.2:c.462C>T	XP_016870810.1:p.Ser154=
XM_017015323.2:c.-301C>T	XP_016870812.1:n.-301C>T
XM_024447716.1:c.735C>T	XP_024303484.1:p.Ser245=
XM_024447717.1:c.735C>T	XP_024303485.1:p.Ser245=
XR_002956828.1:n.750C>T
XR_002956829.1:n.750C>T
XR_002956830.1:n.521C>T
XR_002956831.1:n.196C>T
XR_002956832.1:n.521C>T
NM_012203.2:c.462C>T MANE Select	NP_036335.1:p.Ser154=