Canonical Allele Identifier: CA374619084

Gene: WHRN

Linked Data

• MyVariant Identifiers: chr9:g.117165209C>G (hg19) ; chr9:g.114402929C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402929C>G , CM000671.2:g.114402929C>G	GRCh38
NC_000009.11:g.117165209C>G , CM000671.1:g.117165209C>G	GRCh37
NC_000009.10:g.116205030C>G	NCBI36
NG_016700.1:g.107528G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.893G>C	ENSP00000514396.1:p.Gly298Ala
ENST00000362057.4:c.2549G>C MANE Select	ENSP00000354623.3:p.Gly850Ala
ENST00000674036.8:c.1522G>C
ENST00000674048.1:n.2430G>C
ENST00000265134.10:c.1400G>C	ENSP00000265134.6:p.Gly467Ala
ENST00000362057.3:c.2549G>C	ENSP00000354623.3:p.Gly850Ala
ENST00000374059.7:c.1496G>C	ENSP00000363172.3:p.Gly499Ala
NM_001083885.2:c.1400G>C	NP_001077354.2:p.Gly467Ala
NM_001173425.1:c.2546G>C	NP_001166896.1:p.Gly849Ala
NM_015404.3:c.2549G>C	NP_056219.3:p.Gly850Ala
XM_005251897.3:c.1886G>C	XP_005251954.2:p.Gly629Ala
XM_011518484.1:c.2582G>C	XP_011516786.1:p.Gly861Ala
XM_011518485.1:c.2582G>C	XP_011516787.1:p.Gly861Ala
XM_011518486.1:c.2579G>C	XP_011516788.1:p.Gly860Ala
XM_011518487.1:c.2456G>C	XP_011516789.1:p.Gly819Ala
XM_011518488.1:c.2339G>C	XP_011516790.1:p.Gly780Ala
XM_011518495.1:c.1259G>C	XP_011516797.1:p.Gly420Ala
XR_929747.1:n.3486G>C
XR_929748.1:n.3384G>C
NM_001346890.1:c.1496G>C	NP_001333819.1:p.Gly499Ala
XM_011518486.2:c.2579G>C	XP_011516788.1:p.Gly860Ala
XM_011518487.2:c.2456G>C	XP_011516789.1:p.Gly819Ala
XM_011518488.2:c.2339G>C	XP_011516790.1:p.Gly780Ala
XR_929747.2:n.2797G>C
XR_929748.2:n.2695G>C
NM_015404.4:c.2549G>C MANE Select	NP_056219.3:p.Gly850Ala
NM_001173425.2:c.2546G>C	NP_001166896.1:p.Gly849Ala
NM_001083885.3:c.1400G>C	NP_001077354.2:p.Gly467Ala