Canonical Allele Identifier: CA383457593

Gene: SNX19

Linked Data

• MyVariant Identifiers: chr11:g.130750528C>G (hg19) ; chr11:g.130880633C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880633C>G , CM000673.2:g.130880633C>G	GRCh38
NC_000011.9:g.130750528C>G , CM000673.1:g.130750528C>G	GRCh37
NC_000011.8:g.130255738C>G	NCBI36
NG_053190.1:g.40856G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2747G>C MANE Select	ENSP00000265909.4:p.Gly916Ala
ENST00000265909.8:c.2747G>C	ENSP00000265909.4:p.Gly916Ala
ENST00000426933.6:c.251G>C	ENSP00000413345.2:p.Gly84Ala
ENST00000526579.5:n.178-922G>C
ENST00000527116.5:n.509G>C
ENST00000528555.5:c.887G>C	ENSP00000435122.1:p.Gly296Ala
ENST00000530330.1:n.483G>C
ENST00000530356.5:c.887G>C	ENSP00000432307.1:p.Gly296Ala
ENST00000533318.5:n.1107G>C
ENST00000534726.5:c.467G>C	ENSP00000433699.1:p.Gly156Ala
NM_001301089.1:c.887G>C	NP_001288018.1:p.Gly296Ala
NM_014758.2:c.2747G>C	NP_055573.2:p.Gly916Ala
XM_005271546.3:c.2574-922G>C	XP_005271603.1:n.2574-922G>C
XM_011542819.1:c.2993G>C	XP_011541121.1:p.Gly998Ala
XM_011542820.1:c.2981G>C	XP_011541122.1:p.Gly994Ala
XM_011542821.1:c.2873G>C	XP_011541123.1:p.Gly958Ala
XM_011542824.1:c.2111G>C	XP_011541126.1:p.Gly704Ala
XM_011542825.1:c.1268G>C	XP_011541127.1:p.Gly423Ala
XM_011542826.1:c.1133G>C	XP_011541128.1:p.Gly378Ala
XM_011542827.1:c.1013G>C	XP_011541129.1:p.Gly338Ala
NM_001347918.1:c.2627G>C	NP_001334847.1:p.Gly876Ala
NM_001347919.1:c.2574-922G>C	NP_001334848.1:n.2574-922G>C
NM_001347922.1:c.1076G>C	NP_001334851.1:p.Gly359Ala
NM_001347923.1:c.1022G>C	NP_001334852.1:p.Gly341Ala
NM_001347924.1:c.767G>C	NP_001334853.1:p.Gly256Ala
NM_001347925.1:c.713G>C	NP_001334854.1:p.Gly238Ala
NM_001347926.1:c.714-922G>C	NP_001334855.1:n.714-922G>C
NM_001347927.1:c.467G>C	NP_001334856.1:p.Gly156Ala
NR_144939.1:n.3380G>C
XM_011542820.2:c.2981G>C	XP_011541122.1:p.Gly994Ala
XM_011542821.3:c.2873G>C	XP_011541123.1:p.Gly958Ala
XM_011542824.2:c.2111G>C	XP_011541126.1:p.Gly704Ala
XM_011542825.2:c.1268G>C	XP_011541127.1:p.Gly423Ala
XM_011542826.2:c.1133G>C	XP_011541128.1:p.Gly378Ala
XM_024448521.1:c.2993G>C	XP_024304289.1:p.Gly998Ala
XR_001747870.1:n.3818G>C
XR_001747872.1:n.3164G>C
XR_001747873.1:n.3478G>C
NM_001301089.2:c.887G>C	NP_001288018.1:p.Gly296Ala
NM_001347918.2:c.2627G>C	NP_001334847.2:p.Gly876Ala
NM_001347919.2:c.2574-922G>C	NP_001334848.2:n.2574-922G>C
NM_001347920.2:c.*21143G>C	NP_001334849.2:n.*21143G>C
NM_001347922.2:c.1076G>C	NP_001334851.2:p.Gly359Ala
NM_001347923.2:c.1022G>C	NP_001334852.2:p.Gly341Ala
NM_001347924.2:c.767G>C	NP_001334853.1:p.Gly256Ala
NM_001347925.2:c.713G>C	NP_001334854.1:p.Gly238Ala
NM_001347926.2:c.714-922G>C	NP_001334855.1:n.714-922G>C
NM_001347927.2:c.467G>C	NP_001334856.1:p.Gly156Ala
NM_014758.3:c.2747G>C MANE Select	NP_055573.3:p.Gly916Ala
NR_144939.2:n.3372G>C