Canonical Allele Identifier: CA382898451

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.118963509G>C (hg19) ; chr11:g.119092799G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092799G>C , CM000673.2:g.119092799G>C	GRCh38
NC_000011.9:g.118963509G>C , CM000673.1:g.118963509G>C	GRCh37
NC_000011.8:g.118468719G>C	NCBI36
NG_008093.1:g.12923G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.648G>C	ENSP00000509288.1:p.Met216Ile
ENST00000691144.1:n.3028G>C
ENST00000691249.1:n.1637G>C
ENST00000442944.7:c.795G>C	ENSP00000392041.3:p.Met265Ile
ENST00000640813.1:c.*50G>C	ENSP00000491061.1:n.*50G>C
ENST00000648026.1:c.707G>C	ENSP00000498044.1:n.707G>C
ENST00000648374.1:c.762G>C	ENSP00000497255.1:p.Met254Ile
ENST00000649823.1:n.1270G>C
ENST00000650101.1:c.744G>C	ENSP00000496970.1:p.Met248Ile
ENST00000650307.1:n.1639G>C
ENST00000652429.1:c.813G>C MANE Select	ENSP00000498786.1:p.Met271Ile
ENST00000278715.7:c.813G>C	ENSP00000278715.3:p.Met271Ile
ENST00000392841.1:c.762G>C	ENSP00000376584.1:p.Met254Ile
ENST00000442944.6:c.762G>C	ENSP00000392041.2:p.Met254Ile
ENST00000537841.5:c.762G>C	ENSP00000444730.1:p.Met254Ile
ENST00000539045.1:n.189G>C
ENST00000542044.5:n.1258G>C
ENST00000542729.5:c.642G>C	ENSP00000443058.1:p.Met214Ile
ENST00000543090.5:c.720G>C	ENSP00000445429.1:p.Met240Ile
ENST00000543543.5:n.1288G>C
ENST00000544182.1:n.1262G>C
ENST00000544387.5:c.693G>C	ENSP00000438424.1:p.Met231Ile
ENST00000546226.5:n.1575G>C
NM_000190.3:c.813G>C	NP_000181.2:p.Met271Ile
NM_001024382.1:c.762G>C	NP_001019553.1:p.Met254Ile
NM_001258208.1:c.693G>C	NP_001245137.1:p.Met231Ile
NM_001258209.1:c.642G>C	NP_001245138.1:p.Met214Ile
XM_005271531.1:c.762G>C	XP_005271588.1:p.Met254Ile
XM_005271532.1:c.762G>C	XP_005271589.1:p.Met254Ile
XM_005271533.2:c.759G>C	XP_005271590.1:p.Met253Ile
XM_011542796.1:c.648G>C	XP_011541098.1:p.Met216Ile
NM_000190.4:c.813G>C MANE Select	NP_000181.2:p.Met271Ile
NM_001024382.2:c.762G>C	NP_001019553.1:p.Met254Ile
XM_005271533.3:c.759G>C	XP_005271590.1:p.Met253Ile
XM_017017629.1:c.762G>C	XP_016873118.1:p.Met254Ile
XM_024448460.1:c.639G>C	XP_024304228.1:p.Met213Ile
NM_001258208.2:c.693G>C	NP_001245137.1:p.Met231Ile
NM_001258209.2:c.642G>C	NP_001245138.1:p.Met214Ile